Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_provenance.
- NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_assertion description "[The two closely linked genes are located on chromosome 6p, between HLA-B and -DR. Several reports have established complete C4B deficiency as the major genetic risk factor for IgA nephropathy (RR = 6.5; p = 0.0004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_provenance.
- NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_assertion evidence source_evidence_literature NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_provenance.
- NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_assertion SIO_000772 2573592 NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_provenance.
- NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_assertion wasDerivedFrom befree-20150227 NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_provenance.
- NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_assertion wasGeneratedBy ECO_0000203 NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP451683.RA3nLCrYv_gMpYpVM6-VS7BTSUdXd2g7zTmn60CyomPXw130_provenance.