Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_provenance.
- NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_assertion description "[Renal amyloidosis has been considered rare and late in the evolution of the transthyretin (TTR) familial amyloid polyneuropathy (FAP) of the Portuguese type (type I).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_provenance.
- NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_assertion evidence source_evidence_literature NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_provenance.
- NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_assertion SIO_000772 9631837 NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_provenance.
- NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_assertion wasDerivedFrom befree-2016 NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_provenance.
- NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_assertion wasGeneratedBy ECO_0000203 NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_provenance.
- befree-2016 importedOn "2016-02-19" NP1397621.RACS4L-2WpTQV4wBmmo7lTI5kuSQbpjVTTtLkXYJLOB90130_provenance.