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- NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_assertion type Assertion NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_head.
- NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_provenance.
- NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_assertion evidence source_evidence_literature NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_provenance.
- NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_assertion SIO_000772 18309337 NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_provenance.
- NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_assertion wasDerivedFrom befree-20140225 NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_provenance.
- NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_assertion wasGeneratedBy ECO_0000203 NP499188.RA-sAvifeIjsrnOGtJHnk8uP8bKIxnh9ofx1SsS969cSY130_provenance.