Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_provenance.
- NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_assertion description "[Mutations in ALDH4A1 are associated with type II hyperprolinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_provenance.
- NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_assertion evidence source_evidence_literature NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_provenance.
- NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_assertion SIO_000772 10971205 NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_provenance.
- NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_assertion wasDerivedFrom befree-20140225 NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_provenance.
- NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_assertion wasGeneratedBy ECO_0000203 NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP617915.RAgNxvSxsZhVL_OE0_05TWj7AtSjdOk-wp5KbuzM3nxVU130_provenance.