Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_provenance.
- NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_assertion wasGeneratedBy ECO_0000203 NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_provenance.
- NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_assertion wasDerivedFrom befree-20150227 NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_provenance.
- NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_assertion SIO_000772 22490426 NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_provenance.
- NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_assertion evidence source_evidence_literature NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_provenance.
- NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_assertion description "[Pelizaeus-Merzbacher disease (PMD; MIM#312080) is a rare X-linked leukodystrophy presenting with motor developmental delay associated with spasticity and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631408.RAFL6tldSVXQb04SmQnegRAtl5m3NT-b-A3S2v1dzdfGk130_provenance.