Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_assertion wasGeneratedBy ECO_0000203 NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_assertion wasDerivedFrom befree-20150227 NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_assertion SIO_000772 23539225 NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_assertion evidence source_evidence_literature NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.
- NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_assertion description "[Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725067.RAnzhUXULpYMZ-3qxyqk13ed52CDFi42hI6LT1S_lpZQ8130_provenance.