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- source_evidence_literature type ECO_0000212 NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_provenance.
- NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_assertion wasGeneratedBy ECO_0000203 NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_provenance.
- NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_assertion wasDerivedFrom befree-20140225 NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_provenance.
- NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_assertion SIO_000772 8614119 NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_provenance.
- NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_assertion evidence source_evidence_literature NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_provenance.
- NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_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." NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_provenance.
- befree-20140225 importedOn "2014-02-25" NP463051.RA97b1eSlJ4ioxPR9Wjfbdnn8kfVSN89WP25BPA8aNs34130_provenance.