Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_assertion> ?p ?o ?g. }
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- NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_assertion type Assertion NP107563.RAgTdC1rs1Gr1zxE93OoDpU5EeeojK7RJFQHF_SwLEKgI130_head.
- 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.