Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_assertion> ?p ?o ?g. }
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- NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_assertion type Assertion NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_head.
- NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_assertion description "[Charcot-Marie-Tooth neuropathy (CMT) type 1 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." NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_provenance.
- NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_assertion evidence source_evidence_literature NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_provenance.
- NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_assertion SIO_000772 7804455 NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_provenance.
- NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_assertion wasDerivedFrom befree-20140225 NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_provenance.
- NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_assertion wasGeneratedBy ECO_0000203 NP211261.RA5loykT3j2UEOJKN8wGUzvVYM3oSSJRVtV6U-u2MzrIs130_provenance.