Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance.
- NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_assertion wasGeneratedBy ECO_0000203 NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance.
- NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_assertion wasDerivedFrom befree-20150227 NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance.
- NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_assertion SIO_000772 23886208 NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance.
- NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_assertion evidence source_evidence_literature NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance.
- NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_assertion description "[However, the specific combination of GSTM1 null, GSTT1 null, and CYP1B1 codon 119 risk allele carriers and specific combination of GSTM1 present, GSTT1 null, and CYP1B1 432 risk allele carriers exhibited increased cancer risk in the combined analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance.