Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_provenance.
- NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_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." NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_provenance.
- NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_assertion evidence source_evidence_literature NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_provenance.
- NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_assertion SIO_000772 15671604 NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_provenance.
- NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_assertion wasDerivedFrom befree-2016 NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_provenance.
- NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_assertion wasGeneratedBy ECO_0000203 NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_provenance.
- befree-2016 importedOn "2016-02-19" NP478047.RAv98OWJ_to8q8WPUwXVyyrxDE1vWaRC19cHkWrNm69_0130_provenance.