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- NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_assertion type Assertion NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_head.
- NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_provenance.
- NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_assertion evidence source_evidence_literature NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_provenance.
- NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_assertion SIO_000772 10581037 NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_provenance.
- NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_assertion wasDerivedFrom befree-20150227 NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_provenance.
- NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_assertion wasGeneratedBy ECO_0000203 NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_provenance.