Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_provenance.
- NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_assertion wasGeneratedBy ECO_0000203 NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_provenance.
- NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_assertion wasDerivedFrom befree-2016 NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_provenance.
- NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_assertion SIO_000772 9241277 NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_provenance.
- NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_assertion evidence source_evidence_literature NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_provenance.
- NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_assertion description "[Family studies showed that an Arg145Gly mutation was linked to HCM and a Lys206Gln mutation had occurred de novo, thus strongly suggesting that cTnI is the seventh HCM gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1377588.RAZdGqKRTHRXbysytnPd6BmJRyxKG1ELQn9TIfmWVt3Tc130_provenance.