Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_provenance.
- NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_assertion description "[Identification of seven novel mutations in ABCD1 by a DHPLC-based assay in Italian patients with X-linked adrenoleukodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_provenance.
- NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_assertion evidence source_evidence_curated NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_provenance.
- NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_assertion SIO_000772 15643618 NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_provenance.
- NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_assertion wasDerivedFrom uniprot-20130724 NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_provenance.
- NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_assertion wasGeneratedBy ECO_0000218 NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP100.RAnzNBxrEWifkLRV6RTAHAYcO8jg0UoJqXAq1okudzA6M130_provenance.