Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_provenance.
- NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_assertion description "[The GSTM1 deletion and the variant (GG) genotype of the CYP1B1 rs1800440 polymorphism were associated with a decreased risk of developing endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_provenance.
- NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_assertion evidence source_evidence_literature NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_provenance.
- NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_assertion SIO_000772 20381444 NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_provenance.
- NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_assertion wasDerivedFrom befree-20140225 NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_provenance.
- NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_assertion wasGeneratedBy ECO_0000203 NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP256915.RApKpA5ngb6A2p0g0ALLI1f1Wheeb8Psu_psiDhgFvuSc130_provenance.