Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_provenance.
- NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_assertion wasGeneratedBy ECO_0000203 NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_provenance.
- NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_assertion wasDerivedFrom befree-20140225 NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_provenance.
- NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_assertion SIO_000772 8614119 NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_provenance.
- NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_assertion evidence source_evidence_literature NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_provenance.
- NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_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." NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP667621.RASe-w1tCTyCrsxcLOx5jvtRx5CCipZs6AoJanvRxwsG8130_provenance.