Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance.
- NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_assertion description "[Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance.
- NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_assertion evidence source_evidence_literature NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance.
- NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_assertion SIO_000772 19388158 NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance.
- NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_assertion wasDerivedFrom befree-2016 NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance.
- NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_assertion wasGeneratedBy ECO_0000203 NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance.
- befree-2016 importedOn "2016-02-19" NP734254.RAcIHiQj8qciH71YwTZyc__o6Q66ap7gkEVA4-nVHT0PE130_provenance.