Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_assertion> ?p ?o ?g. }
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- NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_assertion type Assertion NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_head.
- NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_assertion wasGeneratedBy ECO_0000203 NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_provenance.
- NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_assertion wasDerivedFrom befree-20150227 NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_provenance.
- NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_assertion SIO_000772 22488412 NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_provenance.
- NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_assertion evidence source_evidence_literature NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_provenance.
- NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_assertion description "[All patients with an NKX2.1 mutation had BHC and congenital hypothyroidism, emphasizing the high prevalence of these signs associated with defective NKX2.1 alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739214.RADsgPbLC5UqO6EZ5jmCNnibCiUQ2COs8E_3jcnlrb1pU130_provenance.