Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance.
- NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance.
- NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_assertion evidence source_evidence_literature NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance.
- NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_assertion SIO_000772 2564060 NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance.
- NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_assertion wasDerivedFrom befree-2016 NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance.
- NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_assertion wasGeneratedBy ECO_0000203 NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance.