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- NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_assertion type Assertion NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_head.
- NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_assertion wasGeneratedBy ECO_0000203 NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_provenance.
- NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_assertion wasDerivedFrom befree-20150227 NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_provenance.
- NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_assertion SIO_000772 16505158 NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_provenance.
- NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_assertion evidence source_evidence_literature NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_provenance.
- NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_assertion description "[CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2), although mutations have also been detected in patients with divergent diagnoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277411.RAifzixpqCS58Npfn_IzneDCCy2g-vdbHTXs3ltOYNVjc130_provenance.