Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_assertion> ?p ?o ?g. }
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- NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_assertion type Assertion NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_head.
- NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_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." NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_provenance.
- NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_assertion evidence source_evidence_literature NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_provenance.
- NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_assertion SIO_000772 21738389 NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_provenance.
- NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_assertion wasDerivedFrom befree-20140225 NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_provenance.
- NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_assertion wasGeneratedBy ECO_0000203 NP871211.RAs4jWxpWK3oBg5A7RZFuhgfCZmgLWmHHXUBjDKGZkYw0130_provenance.