Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance.
- NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_assertion wasGeneratedBy ECO_0000218 NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance.
- NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_assertion wasDerivedFrom uniprot-2016 NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance.
- NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_assertion SIO_000772 12406339 NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance.
- NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_assertion evidence source_evidence_curated NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance.
- NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_assertion description "[A novel missense mutation affecting the human hairless thyroid receptor interacting domain 2 causes congenital atrichia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance.