Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_provenance.
- NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_assertion description "[We present a Finnish family with familial amyloidotic polyneuropathy (FAP Met30), a type of amyloidosis hitherto not described in the Finnish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_provenance.
- NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_assertion evidence source_evidence_literature NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_provenance.
- NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_assertion SIO_000772 1511998 NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_provenance.
- NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_assertion wasDerivedFrom befree-2016 NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_provenance.
- NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_assertion wasGeneratedBy ECO_0000203 NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_provenance.
- befree-2016 importedOn "2016-02-19" NP442225.RAgPq_tQ4vzvaL56d6iWHdhGhOcKA6NXEVROAFJI6F9QY130_provenance.