Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_provenance.
- NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_assertion description "[Mutations in NPHS2 (podocin) in Mexican children with nephrotic syndrome who respond to standard steroid treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_provenance.
- NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_assertion evidence source_evidence_literature NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_provenance.
- NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_assertion SIO_000772 23913389 NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_provenance.
- NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_assertion wasDerivedFrom befree-20150227 NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_provenance.
- NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_assertion wasGeneratedBy ECO_0000203 NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP783733.RAQ18fUWkk8bRMK2_i6mE8yifVxoQ8ONx-b2BVXUYfphI130_provenance.