@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:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_head { this: np:hasAssertion dgn-np:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_assertion; np:hasProvenance dgn-np:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_provenance; np:hasPublicationInfo dgn-np:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_publicationInfo; a np:Nanopublication . dgn-np:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_assertion a np:Assertion . dgn-np:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_provenance a np:Provenance . dgn-np:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_publicationInfo a np:PublicationInfo . } dgn-np:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_assertion { miriam-gene:282617 a ncit:C16612 . lld:C0015695 a ncit:C7057 . dgn-gda:DGNde43d4731c7e5da4d7ecd045268c095f sio:SIO_000628 miriam-gene:282617, lld:C0015695; a sio:SIO_001121 . } dgn-np:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_provenance { dgn-np:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_assertion dcterms:description "[A sustained virological response (SVR) was significantly associated with IL28B polymorphism (CC vs TT allele: odds ratio (OR), 25; CC vs CT allele: OR, 5.4), inflammation activity (G < 1 vs G > 1: OR, 3.9), fibrosis (F < 1 vs F > 1: OR, 5.9), platelet count (> 200 × 10(9)/L vs < 200 × 10(9)/L: OR, 4.7; OR in patients with genotype CT: 12.8), fatty liver (absence vs presence of steatosis: OR, 4.8), insulin resistance index (< 2.5 vs > 2.5: OR, 3.9), and baseline HCV viral load (< 10(6) IU/mL vs > 10(6) IU/mL: OR, 3.0).]. 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:23002361; 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:NP1015271.RAs3UdS0j_yrqkw8-1Hx-KqKs8Uvvf8fWBSrf_yzF1gWo130_publicationInfo { this: dcterms:created "2016-05-13T12:49:26+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" . }