Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance.
- NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_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." NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance.
- NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_assertion evidence source_evidence_literature NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance.
- NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_assertion SIO_000772 16076902 NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance.
- NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_assertion wasDerivedFrom befree-20150227 NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance.
- NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_assertion wasGeneratedBy ECO_0000203 NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP842800.RAbC0R7Qr1q6qKoLkY6p-t-YPNHn2P8s7-mAoU1YPhBQ0130_provenance.