@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:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_head { this: np:hasAssertion dgn-np:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_assertion; np:hasProvenance dgn-np:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_provenance; np:hasPublicationInfo dgn-np:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_publicationInfo; a np:Nanopublication . dgn-np:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_assertion a np:Assertion . dgn-np:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_provenance a np:Provenance . dgn-np:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_publicationInfo a np:PublicationInfo . } dgn-np:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_assertion { miriam-gene:1378 a ncit:C16612 . lld:C0024534 a ncit:C7057 . dgn-gda:DGNf56aae63d3ec0d74094b853ff08533d8 sio:SIO_000628 miriam-gene:1378, lld:C0024534; a sio:SIO_001122 . } dgn-np:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_provenance { dgn-np:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_assertion dcterms:description "[We found a higher frequency of HL and AA phenotypes in the study subjects. Our findings are unique as we found that gene frequencies for structural and quantitative polymorphism in our study subjects were a combination of those found in Caucasian and Orie]. 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:14556965; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP82035.RAn-ji6nn-CljbhQXynq9tr7140IVUeyxIwhOvgPT46K8130_publicationInfo { this: dcterms:created "2016-05-13T12:42:25+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }