Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_assertion> ?p ?o ?g. }
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- NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_assertion type Assertion NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_head.
- 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.