Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_provenance.
- NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_assertion description "[In oxaliplatin-treated patients, carriers of one or two T variants of Asn118Asn ERCC1 SNP had a lower risk for neutropenia(OR = 0.205; 95 % CI = 0.061?0.690; P = 0.01) [corrected].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_provenance.
- NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_assertion evidence source_evidence_literature NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_provenance.
- NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_assertion SIO_000772 23543295 NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_provenance.
- NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_assertion wasDerivedFrom befree-20150227 NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_provenance.
- NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_assertion wasGeneratedBy ECO_0000203 NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP381368.RAeejW03ThBwZW3a_6fb-FrrD2RVQ7qUhDzJ21njpRBw4130_provenance.