Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_assertion> ?p ?o ?g. }
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- NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_assertion type Assertion NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_head.
- NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_assertion description "[To report novel spectral domain optical coherence tomography (SD-OCT) findings and new mutational data in patients with 'cone dystrophy with supernormal rod electroretinogram', a recessive childhood onset retinal dystrophy consequent upon mutation in the KCNV2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance.
- NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_assertion evidence source_evidence_literature NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance.
- NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_assertion SIO_000772 21558291 NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance.
- NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_assertion wasDerivedFrom befree-20150227 NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance.
- NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_assertion wasGeneratedBy ECO_0000203 NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance.