Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance.