Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_provenance.
- NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_assertion description "[In exploring two-way gene interactions, we found a markedly elevated risk for the combination of the XPD codon 312 Asn/Asn and XRCC1 codon 399 Gln/Gln genotypes (OR, 4.81; 95% CI, 1.66-13.97).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_provenance.
- NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_assertion evidence source_evidence_literature NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_provenance.
- NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_assertion SIO_000772 14744728 NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_provenance.
- NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_assertion wasDerivedFrom befree-2016 NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_provenance.
- NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_assertion wasGeneratedBy ECO_0000203 NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_provenance.
- befree-2016 importedOn "2016-02-19" NP429551.RAGN2wEu8U1i797q7xMbPESsVYQCisCQctD1bmc5PIdn0130_provenance.