Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_assertion type Assertion NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_head.
- NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_assertion description "[Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_provenance.
- NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_assertion evidence source_evidence_curated NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_provenance.
- NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_assertion SIO_000772 20206331 NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_provenance.
- NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_assertion wasDerivedFrom uniprot-2016 NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_provenance.
- NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_assertion wasGeneratedBy ECO_0000218 NP6137.RAFDitilIExvBTGMy5QiHL5VPHKCc_2n7yjkNZs0iEbho130_provenance.