Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_provenance.
- NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_assertion description "[An examination of the genetic background and phenotypic presentation of familial hypertrophic cardiomyopathy (FHC) with respect to specific mutations in the MYH7-gene encoding the cardiac beta-myosin heavy chain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_provenance.
- NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_assertion evidence source_evidence_literature NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_provenance.
- NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_assertion SIO_000772 11214007 NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_provenance.
- NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_assertion wasDerivedFrom befree-20140225 NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_provenance.
- NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_assertion wasGeneratedBy ECO_0000203 NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP581942.RAJpcnP7gMHNEbFap1xcJhLngqUaGYxjfkZ9L6xl8oKlM130_provenance.