Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance.
- NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_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." NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance.
- NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_assertion evidence source_evidence_literature NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance.
- NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_assertion SIO_000772 21738389 NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance.
- NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_assertion wasDerivedFrom befree-20150227 NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance.
- NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_assertion wasGeneratedBy ECO_0000203 NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP990345.RAayjwggoP4pOjmRmFE5SgxWm09p09hm70yXezCmz7PP4130_provenance.