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- NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_assertion type Assertion NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_head.
- NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_assertion description "[A novel missense SNRNP200 mutation associated with autosomal dominant retinitis pigmentosa in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_provenance.
- NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_assertion evidence source_evidence_literature NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_provenance.
- NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_assertion SIO_000772 23029027 NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_provenance.
- NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_assertion wasDerivedFrom befree-2016 NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_provenance.
- NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_assertion wasGeneratedBy ECO_0000203 NP1017321.RA-wQxBei_ywnwSVmScBCBYeifURkmQJbORmM6wlHDKaQ130_provenance.