@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:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_head { this: np:hasAssertion dgn-np:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_assertion; np:hasProvenance dgn-np:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_provenance; np:hasPublicationInfo dgn-np:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_publicationInfo; a np:Nanopublication . dgn-np:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_assertion a np:Assertion . dgn-np:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_provenance a np:Provenance . dgn-np:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_publicationInfo a np:PublicationInfo . } dgn-np:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_assertion { miriam-gene:6570 a ncit:C16612 . lld:C0011570 a ncit:C7057 . dgn-gda:DGNeaa29e3562e29dbe98f5a06600ec342b sio:SIO_000628 miriam-gene:6570, lld:C0011570; a sio:SIO_001121 . } dgn-np:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_provenance { dgn-np:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_assertion dcterms:description "[Molecular genetics and developmental studies have identified 21 genes in this region (ADRA1A, ARHGEF10, CHRNA2, CHRNA6, CHRNB3, DKK4, DPYSL2, EGR3, FGF17, FGF20, FGFR1, FZD3, LDL, NAT2, NEF3, NRG1, PCM1, PLAT, PPP3CC, SFRP1 and VMAT1/SLC18A1) that are most likely to contribute to neuropsychiatric disorders (schizophrenia, autism, bipolar disorder and depression), neurodegenerative disorders (Parkinson's and Alzheimer's disease) and cancer.]. 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:19204725; 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:NP719525.RAKKf-lE4R-0F7MmibKan8C0_EAvAcrpnJpmxJOlTGQTA130_publicationInfo { this: dcterms:created "2016-05-13T12:47:11+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" . }