Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_assertion type Assertion NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_head.
- NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_provenance.
- NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_assertion evidence source_evidence_literature NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_provenance.
- NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_assertion SIO_000772 18429043 NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_provenance.
- NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_assertion wasDerivedFrom befree-20140225 NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_provenance.
- NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_assertion wasGeneratedBy ECO_0000203 NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_provenance.