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- source_evidence_literature type ECO_0000212 NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_provenance.
- NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_assertion description "[All patients with the CXCR4 T allele and 16 out of 48 with wild type genotype presented with grade III of MM according to the International Staging System (ISS) (p=0.047).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_provenance.
- NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_assertion evidence source_evidence_literature NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_provenance.
- NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_assertion SIO_000772 23711392 NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_provenance.
- NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_assertion wasDerivedFrom befree-2016 NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_provenance.
- NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_assertion wasGeneratedBy ECO_0000203 NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1081050.RAANs6HJSHOQo7f9n6TyGbfTfwtXf0lO1-03BYpEQwmUU130_provenance.