Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_provenance.
- NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_assertion description "[Mutations in genes encoding myosin VIIa, harmonin, cadherin 23, protocadherin 15 or sans cause Usher syndrome type I (USH1, characterized by congenital deafness, vestibular dysfunction and retinitis pigmentosa leading to blindness) in humans and hair bundle disorganization in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_provenance.
- NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_assertion evidence source_evidence_literature NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_provenance.
- NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_assertion SIO_000772 18339676 NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_provenance.
- NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_assertion wasDerivedFrom befree-20140225 NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_provenance.
- NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_assertion wasGeneratedBy ECO_0000203 NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697279.RAUWFpr5N-i6VtVs1tSrLqgK0ng9wQZj3mBMxQmaR7RNM130_provenance.