Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_provenance.
- NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_assertion description "[Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_provenance.
- NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_assertion evidence source_evidence_curated NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_provenance.
- NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_assertion SIO_000772 10700177 NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_provenance.
- NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_assertion wasDerivedFrom uniprot-20150221 NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_provenance.
- NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_assertion wasGeneratedBy ECO_0000218 NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP271.RAgKlOkyeMCLD4-7BlAyYdLxtFo0-QWhIv6DtH902K7rU130_provenance.