Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_provenance.
- NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_assertion description "[Although there are approximately 100 known TTR variants associated with peripheral neuropathy, in Israel only one patient with familial amyloid polyneuropathy (FAP), a patient of Ashkenazi origin with ATTR due to an F33I mutation, has been reported so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_provenance.
- NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_assertion evidence source_evidence_literature NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_provenance.
- NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_assertion SIO_000772 17484624 NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_provenance.
- NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_assertion wasDerivedFrom befree-2016 NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_provenance.
- NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_assertion wasGeneratedBy ECO_0000203 NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP608598.RAn7NK-lsmXDR3CxPVWYbVcyhPb5aZWY5lpRLeUwsyqvQ130_provenance.