Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion type Assertion NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_head.
- NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion wasGeneratedBy ECO_0000203 NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.
- NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion wasDerivedFrom befree-2016 NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.
- NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion SIO_000772 21480433 NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.
- NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion evidence source_evidence_literature NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.
- NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion description "[Although mutations in MYH14 have been shown to cause nonsyndromic autosomal dominant hearing loss (DFNA4), the peripheral neuropathy, myopathy, and hoarseness have not been associated with MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.