Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_provenance.
- NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_assertion description "[Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_provenance.
- NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_assertion evidence source_evidence_curated NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_provenance.
- NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_assertion SIO_000772 9589637 NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_provenance.
- NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_assertion wasDerivedFrom uniprot-20130724 NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_provenance.
- NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_assertion wasGeneratedBy ECO_0000218 NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP303.RAKvj4Gdx_rg6OPkg1l2Shs7QEyiOf20ZFnywqA7zUB5I130_provenance.