Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion description "[Hypertrophic cardiomyopathy (HCM) is the most common genetic heart disease and is often a consequence of mutations in the myosin-binding protein C gene (MYBPC3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion evidence source_evidence_literature NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion SIO_000772 16566405 NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion wasDerivedFrom befree-20140225 NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion wasGeneratedBy ECO_0000203 NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.