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- NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_assertion type Assertion NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_head.
- NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a genetically heterogeneous group of chronic demyelinating polyneuropathies with loci mapping to chromosome 17 (CMT1A), chromosome 1 (CMT1B), the X chromosome (CMTX) and to another unknown autosome (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_provenance.
- NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_assertion evidence source_evidence_literature NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_provenance.
- NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_assertion SIO_000772 7849745 NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_provenance.
- NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_assertion wasDerivedFrom befree-2016 NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_provenance.
- NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_assertion wasGeneratedBy ECO_0000203 NP1323778.RAiPIBz8FBz1LZwoCEnimnwrsCamJYPZR_LtnA03vp0fg130_provenance.