Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_provenance.
- NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_assertion description "[The genes for familial cases of hypertrophic cardiomyopathy are known to encode members of the sarcomere and to date nine genes have been identified (beta-myosin heavy chain, alpha-tropomyosin, cardiac troponin T, troponin I, myosin binding protein-C, regulatory myosin light chain, essential myosin light chain, cardiac actin, and titin) for this genetically and clinically heterogeneous disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_provenance.
- NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_assertion evidence source_evidence_literature NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_provenance.
- NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_assertion SIO_000772 10980884 NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_provenance.
- NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_assertion wasDerivedFrom befree-20140225 NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_provenance.
- NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_assertion wasGeneratedBy ECO_0000203 NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP388843.RAONoaDx0tTeHgvgM3xcRJgLgGEVCLgLx9qSGafZwYTTQ130_provenance.