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- NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_assertion type Assertion NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_head.
- NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_assertion description "[Mutations in CRB1 are associated with a range of recessively inherited retinal dystrophies, including LCA, childhood- and juvenile-onset rod-cone and cone-rod dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_provenance.
- NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_assertion evidence source_evidence_literature NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_provenance.
- NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_assertion SIO_000772 20956273 NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_provenance.
- NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_assertion wasDerivedFrom befree-2016 NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_provenance.
- NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_assertion wasGeneratedBy ECO_0000203 NP846507.RAMGLq0738lUP9DT--ANdIPDkkkIjSyCLtfqAxRNov_b0130_provenance.