http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#head http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#assertion http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#provenance http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#assertion http://rdf.disgenet.org/resource/gda/DGN2668ddca9ad4a2f3e952443d6c24ac20 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/64324 http://rdf.disgenet.org/resource/gda/DGN2668ddca9ad4a2f3e952443d6c24ac20 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0175695 http://rdf.disgenet.org/resource/gda/DGN2668ddca9ad4a2f3e952443d6c24ac20 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#provenance http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#assertion http://purl.org/dc/terms/description [Our findings suggest that Sotos syndrome is a rare cause of autism spectrum disorders and that screening for NSD1 mutations and deletions in patients with autism and macrocephaly is not warranted in the absence of other features of Sotos syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#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/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/18001468 http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#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/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/dc/terms/created 2017-10-17T13:18:50+02:00 http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1361942.RA-_qfiaVUJQo3zVC2_qsJD2cp4t3N5aXXD4bBSXJadIQ 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