Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_assertion> ?p ?o ?g. }
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- NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_assertion type Assertion NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_head.
- NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_assertion description "[CMT2A is an axonal autosomal dominant CMT type which in most cases is characterized by early onset and rather severe course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_provenance.
- NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_assertion evidence source_evidence_literature NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_provenance.
- NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_assertion SIO_000772 25847151 NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_provenance.
- NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_assertion wasDerivedFrom befree-2016 NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_provenance.
- NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_assertion wasGeneratedBy ECO_0000203 NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_provenance.