Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_assertion> ?p ?o ?g. }
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- NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_assertion type Assertion NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_head.
- NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_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." NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_provenance.
- NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_assertion evidence source_evidence_literature NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_provenance.
- NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_assertion SIO_000772 7849745 NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_provenance.
- NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_assertion wasDerivedFrom befree-2016 NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_provenance.
- NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_assertion wasGeneratedBy ECO_0000203 NP1323775.RAkH71dxwojODnogSC5JLavaGwZfDcU8FNnXDFb-OCDz4130_provenance.