@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_head { this: np:hasAssertion dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_assertion; np:hasProvenance dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_provenance; np:hasPublicationInfo dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_publicationInfo; a np:Nanopublication . dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_assertion a np:Assertion . dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_provenance a np:Provenance . dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_publicationInfo a np:PublicationInfo . } dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_assertion { miriam-gene:2334 a ncit:C16612 . lld:C0018817 a ncit:C7057 . dgn-gda:DGN108c4f630d7e7069a649a73931d00e55 sio:SIO_000628 miriam-gene:2334, lld:C0018817; a sio:SIO_001121 . } dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_provenance { dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_assertion dcterms:description "[A literature search for genes that have been implicated in ASD yielded 14 candidate genes (OXTR, SHANK3, BCL2, RORA, EN2, RELN, MECP2, AUTS2, NLGN3, NRXN1, SLC6A4, UBE3A, GABA, AFF2) that were epigenetically modified in relation to ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:25687563; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1264236.RA0KYW4IDPc47KaafVpT9Knx9NndNlq5mBlEfszdzWA2Q130_publicationInfo { this: dcterms:created "2016-05-13T12:51:19+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }