Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_provenance.
- NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_assertion description "[Carriers of autosomal-recessive and X-linked Alport syndrome often have a thinned glomerular basement membrane (GBM) and have mutations in the COL4A3/COL4A4 and COL4A5 genes respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_provenance.
- NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_assertion evidence source_evidence_literature NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_provenance.
- NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_assertion SIO_000772 11473630 NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_provenance.
- NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_assertion wasDerivedFrom befree-2016 NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_provenance.
- NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_assertion wasGeneratedBy ECO_0000203 NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_provenance.
- befree-2016 importedOn "2016-02-19" NP325151.RACRc4PrxHiAbdcyjij1y7dCQMhIVyCqamA_hgmpnAdcw130_provenance.