Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_provenance.
- NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_assertion description "[Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_provenance.
- NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_assertion evidence source_evidence_literature NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_provenance.
- NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_assertion SIO_000772 17803723 NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_provenance.
- NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_assertion wasDerivedFrom befree-20140225 NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_provenance.
- NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_assertion wasGeneratedBy ECO_0000203 NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP868961.RARSZKhT5dcAL8LHGRveO5PpwxlwF0R0RlK4tTm8kfDeI130_provenance.