Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion type Assertion NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_head.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion description "[X-linked dominant Charcot-Marie-Tooth disease with connexin 32 (Cx32) mutations in Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion evidence source_evidence_literature NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion SIO_000772 21291455 NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion wasDerivedFrom befree-2016 NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion wasGeneratedBy ECO_0000203 NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.