http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#head
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#assertion
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#provenance
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#assertion
http://rdf.disgenet.org/resource/gda/DGNf61d7e6fcf118af45a1ba1d03677dbf6
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/152330
http://rdf.disgenet.org/resource/gda/DGNf61d7e6fcf118af45a1ba1d03677dbf6
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0036572
http://rdf.disgenet.org/resource/gda/DGNf61d7e6fcf118af45a1ba1d03677dbf6
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#provenance
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#assertion
http://purl.org/dc/terms/description
[We focused our initial analysis on CNTNAP2 based on our demonstration of disruption of Contactin 4 (CNTN4) in a patient with ASD; the recent finding of rare homozygous mutations in CNTNAP2 leading to intractable seizures and autism; and in situ and biochemical analyses reported herein that confirm expression in relevant brain regions and demonstrate the presence of CNTNAP2 in the synaptic plasma membrane fraction of rat forebrain lysates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#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/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/18179895
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#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/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/dc/terms/created
2017-10-17T13:19:08+02:00
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1411087.RA0D4gGLvcwQrWptfTx4QPdx1e8a0IlXIeiHk_EudvZzw
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