Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_provenance.
- NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_assertion wasGeneratedBy ECO_0000218 NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_provenance.
- NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_assertion wasDerivedFrom uniprot-2016 NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_provenance.
- NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_assertion SIO_000772 11531804 NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_provenance.
- NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_assertion evidence source_evidence_curated NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_provenance.
- NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_assertion description "[New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1615.RAVePkE5b-DWULZahXmmhqwdzkGwRazrr0fDIjWC82osg130_provenance.