Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion> ?p ?o ?g. }
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- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion type Assertion NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_head.
- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion description "[X-linked Charcot-Marie-Tooth neuropathy (CMTX), which has clinical features similar to CMT1, is associated with mutations in the connexin32 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion evidence source_evidence_literature NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion SIO_000772 10219749 NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion wasDerivedFrom befree-20150227 NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.
- NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_assertion wasGeneratedBy ECO_0000203 NP568292.RAPiuv6fJD5Z_8hq-2N-ReTKx57kFIJUkVebCAVy8n54o130_provenance.