Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_assertion> ?p ?o ?g. }
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- NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_assertion type Assertion NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_head.
- NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_assertion wasGeneratedBy ECO_0000218 NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_provenance.
- NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_assertion wasDerivedFrom uniprot-20130724 NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_provenance.
- NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_assertion SIO_000772 9590296 NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_provenance.
- NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_assertion evidence source_evidence_curated NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_provenance.
- NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_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." NP4798.RAeKOnZgiYmuoD_Ci-lxt5Em8F83gxPE7Mh7kO6B0vVTA130_provenance.