@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:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_head { this: np:hasAssertion dgn-np:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_assertion; np:hasProvenance dgn-np:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_provenance; np:hasPublicationInfo dgn-np:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_publicationInfo; a np:Nanopublication . dgn-np:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_assertion a np:Assertion . dgn-np:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_provenance a np:Provenance . dgn-np:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_publicationInfo a np:PublicationInfo . } dgn-np:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_assertion { miriam-gene:8856 a ncit:C16612 . lld:C0023467 a ncit:C7057 . dgn-gda:DGN0dfa139bd0e518f73d97fad8fd621d20 sio:SIO_000628 miriam-gene:8856, lld:C0023467; a sio:SIO_001121 . } dgn-np:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_provenance { dgn-np:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_assertion dcterms:description "[We used the allelic discrimination method to identify polymorphisms in GSTT1, SULT1C2, CDA, SXR (drug metabolic pathways), XPD, XPA, XPG, ERCC1, TOP2A (DNA repair), VEGF (angiogenesis), and MDR1 (multidrug resistance) genes in 110 adult patients with intermediate-risk AML, enrolled in the CETLAM-99 prospective trial.]. 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:16507781; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP608406.RAsQjn2rFFPONhzVXhDsj37YtgC_LZ9HgfmbmJCFAGyUM130_publicationInfo { this: dcterms:created "2014-10-02T12:38:05+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }