Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_provenance.
- befree-2016 importedOn "2016-02-19" NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_provenance.
- NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_assertion wasGeneratedBy ECO_0000203 NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_provenance.
- NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_assertion wasDerivedFrom befree-2016 NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_provenance.
- NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_assertion SIO_000772 20171226 NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_provenance.
- NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_assertion evidence source_evidence_literature NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_provenance.
- NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_assertion description "[Inherited mutations in the gene coding for the intermediate filament protein desmin have been demonstrated to cause severe skeletal and cardiac myopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794903.RA3hxm3nrLFRES_w5PtAPBWQaBZ6K8yR3DkmrX9kOK3Vc130_provenance.