Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_provenance.
- NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_assertion description "[No significant association was found between p53 codon 72 genotype and the risk to develop adenocarcinoma, SCC or CIN in the Swedish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_provenance.
- NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_assertion evidence source_evidence_literature NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_provenance.
- NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_assertion SIO_000772 11501650 NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_provenance.
- NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_assertion wasDerivedFrom befree-2016 NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_provenance.
- NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_assertion wasGeneratedBy ECO_0000203 NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP326898.RAp35RPBOXEGrtRV_dUtU2BWx00xfk485QtFNDShfplAQ130_provenance.