@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:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_head { this: np:hasAssertion dgn-np:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_assertion; np:hasProvenance dgn-np:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_provenance; np:hasPublicationInfo dgn-np:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_publicationInfo; a np:Nanopublication . dgn-np:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_assertion a np:Assertion . dgn-np:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_provenance a np:Provenance . dgn-np:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_publicationInfo a np:PublicationInfo . } dgn-np:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_assertion { miriam-gene:7054 a ncit:C16612 . lld:C0036341 a ncit:C7057 . dgn-gda:DGN9ce1b2ca19c7df80219b8e6de1859ea2 sio:SIO_000628 miriam-gene:7054, lld:C0036341; a sio:SIO_001121 . } dgn-np:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_provenance { dgn-np:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_assertion dcterms:description "[In a French population we found the rare variant allele in 5 of 94 (5%) unrelated chronic schizophrenic patients and in none of 145 unaffected controls, thus yielding a significant association (p < 0.01) between schizophrenia and the tyrosine hydroxylase gene.]. 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:7583768; 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:NP1313666.RAiaYM2ES5FJ3g7bgWPG5vVh_5w9sAOjSKCiLwUAh1x6w130_publicationInfo { this: dcterms:created "2016-05-13T12:51:41+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" . }