@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:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_head { this: np:hasAssertion dgn-np:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_assertion; np:hasProvenance dgn-np:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_provenance; np:hasPublicationInfo dgn-np:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_publicationInfo; a np:Nanopublication . dgn-np:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_assertion a np:Assertion . dgn-np:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_provenance a np:Provenance . dgn-np:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_publicationInfo a np:PublicationInfo . } dgn-np:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_assertion { miriam-gene:5979 a ncit:C16612 . lld:C0242383 a ncit:C7057 . dgn-gda:DGN9334aaca744ce8265fc861609cfc8fb9 sio:SIO_000628 miriam-gene:5979, lld:C0242383; a sio:SIO_001122 . } dgn-np:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_provenance { dgn-np:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_assertion dcterms:description "[We investigated the prevalence of common polymorphisms that have been associated with diseases, such as atherosclerosis (ALOX5), hypertension (CYP3A5, AGT, GNB3), diabetes (CAPN10, TCF7L2, PTPN22), prostate cancer (DG8S737, rs1447295), Hirschsprung disease (RET), and age-related macular degeneration (CFH, LOC387715).]. 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:18248681; 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:NP128315.RAMYzlLnfdTXFlZhD-XTfNKHJM03YRsTjdnXD7c0tEU3s130_publicationInfo { this: dcterms:created "2015-08-25T14:38:52+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" . }