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- source_evidence_literature type ECO_0000212 NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_provenance.
- NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_assertion description "[With regard to genotype-phenotype correlation, patients with a mutation in the BBS6, BBS10, or BBS12 gene (10 of 33 patients) had more severe renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_provenance.
- NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_assertion evidence source_evidence_literature NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_provenance.
- NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_assertion SIO_000772 20876674 NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_provenance.
- NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_assertion wasDerivedFrom befree-20140225 NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_provenance.
- NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_assertion wasGeneratedBy ECO_0000203 NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP443085.RA48e6RtL6yvXeLMCj7WKjtLbOZB67dHr0fqVOlE1a6KU130_provenance.