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- NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_assertion type Assertion NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_head.
- NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_assertion wasGeneratedBy ECO_0000203 NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_provenance.
- NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_assertion wasDerivedFrom befree-20150227 NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_provenance.
- NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_assertion SIO_000772 11020419 NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_provenance.
- NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_assertion evidence source_evidence_literature NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_provenance.
- NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_assertion description "[Novel mutation in RP2 gene in two brothers with X-linked retinitis pigmentosa and mtDNA mutation of leber hereditary optic neuropathy who showed marked differences in clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674462.RApK6mt7I3c2NkTm1_lNi7gWJ1KpMcjit76Tl1OBC75oA130_provenance.