Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_assertion> ?p ?o ?g. }
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- NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_assertion type Assertion NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_head.
- 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.