Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_provenance.
- NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_assertion description "[A haplotype encompassing the variant allele of DNA repair gene polymorphism ERCC2/XPD Lys751Gln but not the variant allele of Asp312Asn is associated with risk of lung cancer in a northeastern Chinese population]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_provenance.
- NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_assertion evidence source_evidence_literature NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_provenance.
- NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_assertion SIO_000772 17498557 NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_provenance.
- NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_assertion wasDerivedFrom gad-20150221 NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_provenance.
- NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_assertion wasGeneratedBy ECO_0000203 NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_provenance.