Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_provenance.
- befree-2016 importedOn "2016-02-19" NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_provenance.
- NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_assertion wasGeneratedBy ECO_0000203 NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_provenance.
- NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_assertion wasDerivedFrom befree-2016 NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_provenance.
- NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_assertion SIO_000772 1490495 NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_provenance.
- NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_assertion evidence source_evidence_literature NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_provenance.
- NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_assertion description "[Type I familial amyloid polyneuropathy (FAP) is a molecular disorder with a mutation of the transthyretin (TTR) gene, and most patients previously examined were reported to be heterozygous for this mutant gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431426.RASxhj0365uQp2w4uJeJU6JAwDqwG73aMiitSuzSxUmHo130_provenance.