Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_provenance.
- NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_assertion wasGeneratedBy ECO_0000203 NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_provenance.
- NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_assertion wasDerivedFrom befree-20150227 NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_provenance.
- NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_assertion SIO_000772 11673586 NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_provenance.
- NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_assertion evidence source_evidence_literature NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_provenance.
- NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_assertion description "[The clinical spectrum of SCO2 deficiency includes the delayed development of hypertrophic obstructive cardiomyopathy and severe neurogenic muscular atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834242.RABbPk_93N4rGBZnPMa7gsbQPzLZJsCCjX2shz7T3Zgwc130_provenance.