Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the 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.
- NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion evidence source_evidence_literature NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.
- NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion SIO_000772 21480433 NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.
- NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion wasDerivedFrom befree-2016 NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.
- NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_assertion wasGeneratedBy ECO_0000203 NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.
- befree-2016 importedOn "2016-02-19" NP886021.RA_HcfNglNX6OOBUHpC64Xb7nNSLsE5K-a3cY4SibnRtM130_provenance.