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- source_evidence_literature type ECO_0000212 NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_provenance.
- NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_assertion description "[Eight coding SNPs were chosen in ATM (Ser49Cys), BID (Ser56Cys), CASP8 (Asp302His), CASP10 (Val410Ile), LGALS3 (Pro64His), RASSF1 (Ser133Ala), TP53 (Arg72Pro), and TP53AIP1 (Ala7Val), and two non-coding SNPs were selected in BCL2 (-938C/A) and HDM2 (SNP309).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_provenance.
- NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_assertion evidence source_evidence_literature NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_provenance.
- NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_assertion SIO_000772 21396839 NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_provenance.
- NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_assertion wasDerivedFrom befree-2016 NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_provenance.
- NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_assertion wasGeneratedBy ECO_0000203 NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_provenance.
- befree-2016 importedOn "2016-02-19" NP878940.RAYQ25kIY79ZYoc0jInfWmZcMVmUlhnc2WzTziGrEqhQ0130_provenance.