Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_provenance.
- NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_assertion wasGeneratedBy ECO_0000218 NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_provenance.
- NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_assertion wasDerivedFrom uniprot-20130724 NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_provenance.
- NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_assertion SIO_000772 20023659 NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_provenance.
- NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_assertion evidence source_evidence_curated NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_provenance.
- NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_assertion description "[Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3255.RAeIG6IUWDy_roJ0ywMovaN5wE6Xfta2CHs7noK-WQsEE130_provenance.