Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_provenance.
- NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_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." NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_provenance.
- NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_assertion evidence source_evidence_literature NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_provenance.
- NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_assertion SIO_000772 11473630 NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_provenance.
- NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_assertion wasDerivedFrom befree-20140225 NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_provenance.
- NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_assertion wasGeneratedBy ECO_0000203 NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP666990.RAeryj2lgGBehYdQAEF9xf1NQnvtJQFPp2IpNhp0c8Z7M130_provenance.