@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:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_head { this: np:hasAssertion dgn-np:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_assertion; np:hasProvenance dgn-np:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance; np:hasPublicationInfo dgn-np:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_publicationInfo; a np:Nanopublication . dgn-np:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_assertion a np:Assertion . dgn-np:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance a np:Provenance . dgn-np:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_publicationInfo a np:PublicationInfo . } dgn-np:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_assertion { miriam-gene:85358 a ncit:C16612 . lld:C0023015 a ncit:C7057 . dgn-gda:DGNa13455c4d1ec0165c9b83e1bc9751166 sio:SIO_000628 miriam-gene:85358, lld:C0023015; a sio:SIO_001121 . } dgn-np:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance { dgn-np:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_assertion dcterms:description "[A large number of these corresponded to genomic regions or genes (ATP13A4, CDH9, CDH13, CNTNAP2, CTNNA3, DIAPH3, GRIN2A, MDGA2, SHANK3) that have been either associated with ASD for most of them, or involved in speech or language impairment, or in RE.]. 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:22738016; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_publicationInfo { this: dcterms:created "2015-08-25T14:47:25+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }