Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_assertion> ?p ?o ?g. }
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- NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_assertion type Assertion NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_head.
- NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_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." NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_provenance.
- NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_assertion evidence source_evidence_literature NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_provenance.
- NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_assertion SIO_000772 23604902 NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_provenance.
- NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_assertion wasDerivedFrom befree-20150227 NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_provenance.
- NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_assertion wasGeneratedBy ECO_0000203 NP632296.RAr6A-2vS4ceHonvNwexzFGAr1NOMt2ClmmUDZIYcj11s130_provenance.