Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_assertion> ?p ?o ?g. }
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- NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_assertion type Assertion NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_head.
- NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_assertion wasGeneratedBy ECO_0000218 NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_provenance.
- NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_assertion wasDerivedFrom uniprot-20150221 NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_provenance.
- NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_assertion SIO_000772 22246673 NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_provenance.
- NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_assertion evidence source_evidence_curated NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_provenance.
- NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_assertion description "[Mutations in the CLDN14 gene are known to cause autosomal recessive (AR) non-sydromic hearing loss (NSHL) at the DFNB29 locus on chromosome 21q22.13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP579.RAXJCWkJz_E0oqG9BsH_gaHVaDDeIycJIiVErRDqia8AA130_provenance.