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- NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_assertion type Assertion NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_head.
- NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_assertion wasGeneratedBy ECO_0000203 NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_provenance.
- NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_assertion wasDerivedFrom befree-2016 NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_provenance.
- NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_assertion SIO_000772 9541114 NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_provenance.
- NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_assertion evidence source_evidence_literature NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_provenance.
- NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_assertion description "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_provenance.