Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_provenance.
- NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_assertion description "[We genotyped patients with diagnosis of MCS, suspected MCS and Italian healthy controls for allelic variants of cytochrome P450 isoforms (CYP2C9, CYP2C19, CYP2D6, and CYP3A5), UDP-glucuronosyl transferase (UGT1A1), and glutathione S-transferases (GSTP1, GSTM1, and GSTT1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_provenance.
- NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_assertion evidence source_evidence_literature NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_provenance.
- NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_assertion SIO_000772 20430047 NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_provenance.
- NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_assertion wasDerivedFrom gad-20130706 NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_provenance.
- NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_assertion wasGeneratedBy ECO_0000203 NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP88780.RAHHHve1X3Y1Gp4Ljv6iR9HT7wchlxM8hbS1yaHbKuboA130_provenance.