Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_provenance.
- NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_assertion description "[In addition, six novel polymorphisms (G455G, I462I, G736G and IVS 38-8 G>A in COL4A3, and L658L and A1577A in COL4A4) were demonstrated.Many different COL4A3 and COL4A4 mutations cause TBMN and autosomal recessive Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_provenance.
- NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_assertion evidence source_evidence_literature NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_provenance.
- NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_assertion SIO_000772 17216251 NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_provenance.
- NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_assertion wasDerivedFrom befree-20140225 NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_provenance.
- NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_assertion wasGeneratedBy ECO_0000203 NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP330923.RA6ZOXhhCkoOUiMDQNJG6Y-Qx3Qt3EzJpBuhWNHwiIwW0130_provenance.