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- NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_assertion type Assertion NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_head.
- NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_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." NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_provenance.
- NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_assertion evidence source_evidence_curated NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_provenance.
- NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_assertion SIO_000772 23029027 NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_provenance.
- NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_assertion wasDerivedFrom uniprot-20150221 NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_provenance.
- NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_assertion wasGeneratedBy ECO_0000218 NP461.RAEXp-Mf2kDigdlrHA5B9zB6DOM5YvfTbjidBdWeamQ2s130_provenance.