Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_provenance.
- NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_assertion description "[COL4A4 mutation: from familial hematuria to autosomal-dominant or recessive Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_provenance.
- NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_assertion evidence source_evidence_literature NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_provenance.
- NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_assertion SIO_000772 12028435 NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_provenance.
- NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_assertion wasDerivedFrom lhgdn-20090331 NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_provenance.
- NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_assertion wasGeneratedBy ECO_0000203 NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215066.RAW-Oepkf_-f6Jr4rCsL1brfgHEdBAsbgVAi_TC4d6lCU130_provenance.