Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_provenance.
- NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_assertion description "[In this study, we purified the 30-kDa protein from heart extract and identified it as cardiac troponin I (cTnI), encoded by a gene in which mutations can cause familial hypertrophic cardiomyopathy (HCM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_provenance.
- NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_assertion evidence source_evidence_literature NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_provenance.
- NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_assertion SIO_000772 14595408 NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_provenance.
- NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_assertion wasDerivedFrom befree-2016 NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_provenance.
- NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_assertion wasGeneratedBy ECO_0000203 NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_provenance.
- befree-2016 importedOn "2016-02-19" NP418979.RAQUFtH8jDBXynpAsnStPchPZNB8dEUGcPlNZeSbnBWwo130_provenance.