Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance.
- NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance.
- NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_assertion evidence source_evidence_literature NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance.
- NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_assertion SIO_000772 23797140 NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance.
- NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_assertion wasDerivedFrom befree-20140225 NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance.
- NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_assertion wasGeneratedBy ECO_0000203 NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP379144.RAajaEj0u8wO5Twx1L_62zImy2P583L7qQHpO_1GCmRzY130_provenance.