@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:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_head { this: np:hasAssertion dgn-np:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_assertion; np:hasProvenance dgn-np:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_provenance; np:hasPublicationInfo dgn-np:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_assertion a np:Assertion . dgn-np:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_provenance a np:Provenance . dgn-np:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_assertion { miriam-gene:5020 a ncit:C16612 . lld:C1510586 a ncit:C7057 . dgn-gda:DGNb36737d4b2b2b1039037b317a268c583 sio:SIO_000628 miriam-gene:5020, lld:C1510586; a sio:SIO_001121 . } dgn-np:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_provenance { dgn-np:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_assertion dcterms:description "[The oxytocin receptor gene (OXTR) has been studied as a risk factor for autism spectrum disorder (ASD) owing to converging evidence from multiple levels of analysis that oxytocin (OXT) has an important role in the regulation of affiliative behavior and social bonding in both nonhuman mammals and humans.]. 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:25092245; 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:NP1207833.RAXiKe4XfOIM3h5dci8WGI1oDzEx3LVn4uMS2m7Kt_VKQ130_publicationInfo { this: dcterms:created "2016-05-13T12:50:53+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" . }