Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_assertion> ?p ?o ?g. }
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- NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_assertion type Assertion NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_head.
- NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_assertion description "[Mutations in 2 of these genes were shown to cause BFNC (KCNQ3) and hereditary deafness (KCNQ4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_provenance.
- NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_assertion evidence source_evidence_literature NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_provenance.
- NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_assertion SIO_000772 12707061 NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_provenance.
- NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_assertion wasDerivedFrom befree-2016 NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_provenance.
- NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_assertion wasGeneratedBy ECO_0000203 NP391755.RA9yD9HYNC51lLP8R5NI3ATRZDKoE5oBAmzzXC2iwHevo130_provenance.