Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_provenance.
- NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_assertion description "[A novel missense variant C367A and several other mutations were found in familial colorectal cancer DNA suggesting a limited role for this gene in the devlopment of CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_provenance.
- NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_assertion evidence source_evidence_literature NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_provenance.
- NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_assertion SIO_000772 17029639 NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_provenance.
- NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_assertion wasDerivedFrom lhgdn-20090331 NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_provenance.
- NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_assertion wasGeneratedBy ECO_0000203 NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP170196.RANKPmphSvs6YBwvYqWyclBW1LHSpTP8gaLfGdc-aHYhM130_provenance.