Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_provenance.
- NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_assertion description "[The entire coding sequences of 9 genes (MYH7, MYBPC3, TNNI3, TNNT2, MYL2, MYL3, TPM1, ACTC, andTNNC1) were analyzed in 197 unrelated index cases with familial or sporadic hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_provenance.
- NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_assertion evidence source_evidence_literature NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_provenance.
- NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_assertion SIO_000772 12707239 NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_provenance.
- NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_assertion wasDerivedFrom befree-20140225 NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_provenance.
- NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_assertion wasGeneratedBy ECO_0000203 NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_provenance.
- befree-20140225 importedOn "2014-02-25" NP860198.RAfZo0oTzvUfLhoYpXrdOHRvs3Ix3Ih23yEcYLI1Cjido130_provenance.