Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_provenance.
- NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_assertion description "[Male sex [odds ratio (OR): 3.08] and two polymorphic forms of the OATP-2 gene [the 388/411-411 A?G mutation (OR: 3.6) and the 388-411 mutation (OR: 2.4)] increased the risk of neonatal hyperbilirubinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_provenance.
- NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_assertion evidence source_evidence_literature NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_provenance.
- NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_assertion SIO_000772 21500146 NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_provenance.
- NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_assertion wasDerivedFrom befree-20140225 NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_provenance.
- NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_assertion wasGeneratedBy ECO_0000203 NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP434934.RAxG2AxzG3n_RVoGo33-sFmlSP_7_ulmOu29JVtExeKZg130_provenance.