Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_assertion> ?p ?o ?g. }
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- NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_assertion type Assertion NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_head.
- NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_assertion description "[Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_provenance.
- NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_assertion evidence source_evidence_literature NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_provenance.
- NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_assertion SIO_000772 21340161 NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_provenance.
- NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_assertion wasDerivedFrom befree-20150227 NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_provenance.
- NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_assertion wasGeneratedBy ECO_0000203 NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_provenance.