Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_assertion> ?p ?o ?g. }
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- NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_assertion type Assertion NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_head.
- NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_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." NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_provenance.
- NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_assertion evidence source_evidence_literature NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_provenance.
- NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_assertion SIO_000772 7849745 NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_provenance.
- NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_assertion wasDerivedFrom befree-20150227 NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_provenance.
- NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_assertion wasGeneratedBy ECO_0000203 NP568291.RA0UNidCovhsL0GqeDSTIH_VhccB-DYE-MXNINpfUJLxI130_provenance.