Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance.
- NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_assertion description "[We investigated a possible association of two C2093T, C2180T polymorphisms of the megsin gene with the progression of IgAN towards ESRD, as well as the haplotype reconstruction of megsin gene polymorphisms and clinical manifestation of IgAN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance.
- NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_assertion evidence source_evidence_literature NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance.
- NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_assertion SIO_000772 18498720 NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance.
- NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_assertion wasDerivedFrom befree-2016 NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance.
- NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_assertion wasGeneratedBy ECO_0000203 NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance.
- befree-2016 importedOn "2016-02-19" NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance.