Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_provenance.
- NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_assertion description "[A group of 99 unrelated adult patients with DCM (familial n=27, sporadic n=72) were screened for the following genes: cardiac beta-myosin heavy chain, cardiac myosin-binding protein C (MYBPC3), regulatory and essential myosin light chains, alpha cardiac actin, alpha tropomyosin, cardiac troponin T, cardiac troponin I, cardiac troponin C, dystrophin, and lamin A/C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_provenance.
- NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_assertion evidence source_evidence_literature NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_provenance.
- NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_assertion SIO_000772 15671604 NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_provenance.
- NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_assertion wasDerivedFrom befree-20150227 NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_provenance.
- NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_assertion wasGeneratedBy ECO_0000203 NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP221842.RAjhyIB2x0Wn2srr0FUcLjU1SPPXqDAYN-4xrcCFCaU3Q130_provenance.