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- NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_assertion type Assertion NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_head.
- NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_assertion wasGeneratedBy ECO_0000203 NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_provenance.
- NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_assertion wasDerivedFrom befree-20150227 NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_provenance.
- NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_assertion SIO_000772 24405844 NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_provenance.
- NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_assertion evidence source_evidence_literature NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_provenance.
- NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_provenance.