Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_provenance.
- NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_assertion description "[A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_provenance.
- NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_assertion evidence source_evidence_literature NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_provenance.
- NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_assertion SIO_000772 19429631 NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_provenance.
- NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_assertion wasDerivedFrom befree-2016 NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_provenance.
- NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_assertion wasGeneratedBy ECO_0000203 NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_provenance.
- befree-2016 importedOn "2016-02-19" NP737771.RA9hA7G3e8N9sE5xnyNGQT83QgiDsIFUZmKuDW9fdU0H0130_provenance.