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- source_evidence_literature type ECO_0000212 NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_provenance.
- NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_assertion description "[Familial hypertrophic cardiomyopathy (FHC) is an autosomal dominant disease caused by mutations in all of the major sarcomeric proteins, including the ventricular myosin regulatory light-chain (RLC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_provenance.
- NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_assertion evidence source_evidence_literature NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_provenance.
- NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_assertion SIO_000772 16076902 NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_provenance.
- NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_assertion wasDerivedFrom befree-20140225 NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_provenance.
- NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_assertion wasGeneratedBy ECO_0000203 NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP915580.RANLwvlYtYitbn5wB1BeHF8Dej5lO4aBFQtBtaEPTAmJs130_provenance.