Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_assertion type Assertion NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_head.
- NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_assertion wasGeneratedBy ECO_0000203 NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_provenance.
- NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_assertion wasDerivedFrom befree-2016 NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_provenance.
- NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_assertion SIO_000772 9541114 NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_provenance.
- NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_assertion evidence source_evidence_literature NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_provenance.
- NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_assertion description "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_provenance.