Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_provenance.
- NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_assertion wasGeneratedBy ECO_0000218 NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_provenance.
- NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_assertion wasDerivedFrom uniprot-2016 NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_provenance.
- NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_assertion SIO_000772 9590296 NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_provenance.
- NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_assertion evidence source_evidence_curated NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_provenance.
- NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_assertion description "[PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9739.RAR7S7I8e-LjHbvmY8gl5rhCD_tk67oxkoGDEqRwctM2I130_provenance.