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- source_evidence_literature type ECO_0000212 NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_provenance.
- NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_assertion description "[In oxaliplatin-treated patients, carriers of one or two T variants of Asn118Asn ERCC1 SNP had a lower risk for neutropenia(OR = 0.205; 95 % CI = 0.061?0.690; P = 0.01) [corrected].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_provenance.
- NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_assertion evidence source_evidence_literature NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_provenance.
- NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_assertion SIO_000772 23543295 NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_provenance.
- NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_assertion wasDerivedFrom befree-2016 NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_provenance.
- NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_assertion wasGeneratedBy ECO_0000203 NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1065128.RAH-6X7l9tw14zMVSSIp2bTp_KZdoxu4so6Btm3QlAdnI130_provenance.