Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_provenance.
- NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_assertion description "[Hypertrophic cardiomyopathy is due to sarcomeric gene mutations, however, phenocopies with myocardial hypertrophy can be due to triplet-repeat syndromes (Friedreich ataxia and myotonic dystrophy), mitochondrial and metabolic diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_provenance.
- NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_assertion evidence source_evidence_literature NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_provenance.
- NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_assertion SIO_000772 14711353 NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_provenance.
- NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_assertion wasDerivedFrom befree-20140225 NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_provenance.
- NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_assertion wasGeneratedBy ECO_0000203 NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP494450.RAjwJEMZimEXRyVy-tGhQ8U_SOMSAFCoFrSywqlIFrVaU130_provenance.