Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_assertion> ?p ?o ?g. }
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- NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_assertion type Assertion NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_head.
- NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_assertion description "[While four genes have been found to cause over 90�% of genetically identifiable causes of CMT (PMP22, GJB1, MPZ, MFN2), at least 51 genes and loci have been found to cause CMT when mutated, creating difficulties for clinicians to find a genetic subtype for families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_provenance.
- NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_assertion evidence source_evidence_literature NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_provenance.
- NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_assertion SIO_000772 23604902 NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_provenance.
- NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_assertion wasDerivedFrom befree-2016 NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_provenance.
- NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_assertion wasGeneratedBy ECO_0000203 NP1071280.RA81X84g3-onMpx53DyEzGBZjp1oiYe3JAK1ZB_XMk86A130_provenance.