Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance.
- NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_assertion wasGeneratedBy ECO_0000218 NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance.
- NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_assertion wasDerivedFrom uniprot-20130724 NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance.
- NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_assertion SIO_000772 15776429 NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance.
- NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_assertion evidence source_evidence_curated NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance.
- NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_assertion description "[Recently, SIMPLE/LITAF was shown to be responsible for an autosomal dominant demyelinating form of CMT linked to 16p (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance.