Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_provenance.
- NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_assertion wasGeneratedBy ECO_0000203 NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_provenance.
- NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_assertion wasDerivedFrom befree-2016 NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_provenance.
- NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_assertion SIO_000772 8614119 NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_provenance.
- NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_assertion evidence source_evidence_literature NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_provenance.
- NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_assertion description "[Genetic anomalies can be considered the primary cause of myocardial damage in carriers of dystrophinopathic myopathies; myocardial damage shows the same behavior already described in DMD and BMD patients and progresses from preclinical to dilated cardiomyopathy, passing through stages of myocardial hypertrophy or dysrhythmias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1348236.RAA6XVRqysTaSZGRwTg18zVPBzWfKjeCjDljaRCf70ufk130_provenance.