Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_assertion> ?p ?o ?g. }
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- NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_assertion type Assertion NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_head.
- NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_assertion description "[First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_provenance.
- NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_assertion evidence source_evidence_curated NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_provenance.
- NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_assertion SIO_000772 9452087 NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_provenance.
- NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_assertion wasDerivedFrom uniprot-2016 NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_provenance.
- NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_assertion wasGeneratedBy ECO_0000218 NP9621.RAPE9AEURbPnTwXrDi7Hm2JjYSgjEqQFcC69lhq1er4Ug130_provenance.