Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance.
- NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_assertion description "[Known genetic defects were excluded by performing autosomal recessive retinitis pigmentosa (arRP) genotyping microarray analysis and by Sanger sequencing of the coding exons and flanking intronic regions of eyes shut homolog-drosophila (EYS) and chromosome 2 open reading frame 71 (C2orf71).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance.
- NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_assertion evidence source_evidence_literature NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance.
- NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_assertion SIO_000772 21738389 NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance.
- NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_assertion wasDerivedFrom befree-2016 NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance.
- NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_assertion wasGeneratedBy ECO_0000203 NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP907960.RAScGBLz5HoEDM5UgJn9DX30dDXTwuYg_CStBe8dQaG4Y130_provenance.