Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_provenance.
- NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_assertion description "[Although we did not find a significant relationship between the frequency of the Arg/Pro + Pro/Pro genotype of p53 Arg72Pro and susceptibility in PC, there was a combined effect of CXCL12 GA + AA genotype and the p53 72Arg/Pro + Pro/Pro genotype on the frequency of PC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_provenance.
- NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_assertion evidence source_evidence_literature NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_provenance.
- NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_assertion SIO_000772 17785557 NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_provenance.
- NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_assertion wasDerivedFrom gad-20150221 NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_provenance.
- NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_assertion wasGeneratedBy ECO_0000203 NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_provenance.
- gad-20150221 importedOn "2015-02-21" NP75236.RADkFt7KD_408wNed-fGBPeuteNDaOjNpFl82cXtHZG2s130_provenance.