Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_assertion> ?p ?o ?g. }
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- NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_assertion type Assertion NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_head.
- NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_assertion wasGeneratedBy ECO_0000203 NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_provenance.
- NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_assertion wasDerivedFrom befree-2016 NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_provenance.
- NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_assertion SIO_000772 19542741 NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_provenance.
- NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_assertion evidence source_evidence_literature NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_provenance.
- NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_assertion description "[In 80-85% of cases, congenital hypothyroidism is associated with thyroid dysgenesis (TD), but only in a small percentage of cases mutations in thyroid transcription factors (NKX2.1, PAX8, FOXE1, and NKX2.5) have been associated with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP746466.RAOl2-S_2DRHFNCI6WXmU4-CunmNYY2y2vh882vZIDbO4130_provenance.