http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#head http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#assertion http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#provenance http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#assertion http://rdf.disgenet.org/resource/gda/DGN15ff85226040fbb9f164e69270334bfb http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/8910 http://rdf.disgenet.org/resource/gda/DGN15ff85226040fbb9f164e69270334bfb http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0028768 http://rdf.disgenet.org/resource/gda/DGN15ff85226040fbb9f164e69270334bfb http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#provenance http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#assertion http://purl.org/dc/terms/description [As several other uncommon, less well quantitated genetic variations occur with an OCD phenotype, including chromosomal anomalies and some other rare gene variants (SGCE, GCH1 and SLITRK1), a tentative conclusion is that OCD resembles other complex disorders in being etiologically heterogeneous and in having both highly penetrant familial subtypes associated with rare alleles or chromosomal anomalies, as well as having a more common, polygenetic form that may involve polymorphisms in such genes as BDNF, COMT, GRIN2beta, TPH2, HTR2A and SLC1A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/18197083 http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/dc/terms/created 2017-10-17T13:17:37+02:00 http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1166826.RA_XfjHl62ZB4_l2jAuQ6vaMAOCNcfabyMYrcn9lQbib8 http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0