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- source_evidence_literature type ECO_0000212 NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_provenance.
- NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_assertion description "[This study identified a novel disease-causing mutation p.R187C in MIP in a Chinese cataract family, expanding the mutation spectrum of MIP causing congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_provenance.
- NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_assertion evidence source_evidence_literature NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_provenance.
- NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_assertion SIO_000772 21245956 NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_provenance.
- NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_assertion wasDerivedFrom befree-20140225 NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_provenance.
- NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_assertion wasGeneratedBy ECO_0000203 NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP862717.RABnGThFQwC0YlB2mgFi5VEcBQDy_ZV0nHi7jxaBldPNo130_provenance.