@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:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_head { this: np:hasAssertion dgn-np:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_assertion; np:hasProvenance dgn-np:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_provenance; np:hasPublicationInfo dgn-np:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_publicationInfo; a np:Nanopublication . dgn-np:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_assertion a np:Assertion . dgn-np:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_provenance a np:Provenance . dgn-np:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_publicationInfo a np:PublicationInfo . } dgn-np:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_assertion { miriam-gene:2952 a ncit:C16612 . lld:C0205748 a ncit:C7057 . dgn-gda:DGNca6e0df4aca6b150ddd9752c742ebc4c sio:SIO_000628 miriam-gene:2952, lld:C0205748; a sio:SIO_001121 . } dgn-np:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_provenance { dgn-np:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_assertion dcterms:description "[To determine the association between GSTM1 and GSTT1 homozygous deletions (GSTM1 null and GSTT1 null, respectively) and CMM, we studied 212 patients with CMM, 150 patients with CMM and dysplastic nevi (DN), 147 patients with DN alone, and 124 healthy persons without CMM or DN.]. 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:11352862; 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:NP440660.RArAoC0sdipgDk1OMgly4tQZ0JIxwTTjBqsUv5P5lKFf8130_publicationInfo { this: dcterms:created "2015-08-25T14:41:57+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" . }