Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_provenance.
- NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_assertion description "[X-ALD is a neurological disorder associated with inherited defects in the ABCD1 (ALD) gene located on Xq28 and with impaired peroxisomal very long-chain fatty acid beta-oxidation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_provenance.
- NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_assertion evidence source_evidence_literature NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_provenance.
- NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_assertion SIO_000772 11438993 NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_provenance.
- NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_assertion wasDerivedFrom befree-20150227 NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_provenance.
- NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_assertion wasGeneratedBy ECO_0000203 NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP234056.RADRBHxuGyQvc0wUL4yFtDEDocdpib7CHIkgQyerFXmvc130_provenance.