Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_provenance.
- NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_assertion description "[Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_provenance.
- NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_assertion evidence source_evidence_curated NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_provenance.
- NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_assertion SIO_000772 7920658 NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_provenance.
- NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_assertion wasDerivedFrom uniprot-2016 NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_provenance.
- NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_assertion wasGeneratedBy ECO_0000218 NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8621.RA2rMsvDGfd7Dcp43tG8id-H6bK4sUuDzT8npANcRENGI130_provenance.