Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_assertion type Assertion NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_head.
- NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_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." NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_provenance.
- NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_assertion evidence source_evidence_literature NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_provenance.
- NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_assertion SIO_000772 7804455 NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_provenance.
- NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_assertion wasDerivedFrom befree-20140225 NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_provenance.
- NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_assertion wasGeneratedBy ECO_0000203 NP939440.RAp0Zny1SzoOHjr8oQlSpkvYNViplKFbbMXNhYwGcx0o8130_provenance.