Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_provenance.
- NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_assertion description "[It is most frequently seen in patients with hereditary transthyretin (TTR) amyloidosis, but is also present in 20% of patients with systemic immunoglobulin light chain (primary) amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_provenance.
- NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_assertion evidence source_evidence_literature NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_provenance.
- NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_assertion SIO_000772 17554795 NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_provenance.
- NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_assertion wasDerivedFrom befree-20150227 NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_provenance.
- NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_assertion wasGeneratedBy ECO_0000203 NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP761780.RAnyENf0uvYVOF3dP3Ltr34AqmtfqBFCKn2AFi7iVLq1s130_provenance.