Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_provenance.
- NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_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." NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_provenance.
- NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_assertion evidence source_evidence_literature NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_provenance.
- NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_assertion SIO_000772 20876674 NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_provenance.
- NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_assertion wasDerivedFrom befree-20150227 NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_provenance.
- NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_assertion wasGeneratedBy ECO_0000203 NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977637.RAgkJJf_YLbiSVuhamRdd0VkvNuRi8M2CVtII5q3KlgCA130_provenance.