Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_provenance.
- NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_assertion description "[ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_provenance.
- NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_assertion evidence source_evidence_curated NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_provenance.
- NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_assertion SIO_000772 11748843 NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_provenance.
- NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_assertion wasDerivedFrom uniprot-2016 NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_provenance.
- NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_assertion wasGeneratedBy ECO_0000218 NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1767.RAjY14N5ekWdx4lkdth9GdpeUnLP1RKbna8U5RLkmTY5s130_provenance.