Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance.
- NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance.
- NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_assertion evidence source_evidence_literature NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance.
- NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_assertion SIO_000772 16076902 NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance.
- NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_assertion wasDerivedFrom befree-20140225 NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance.
- NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_assertion wasGeneratedBy ECO_0000203 NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP890490.RA0dOj5pZdJ_KyyMe0_qQPsFXHeiJrFOl_0BDD3dPn-sI130_provenance.