Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_assertion type Assertion NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_head.
- NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_assertion wasGeneratedBy ECO_0000203 NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_provenance.
- NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_assertion wasDerivedFrom befree-2016 NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_provenance.
- NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_assertion SIO_000772 20584796 NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_provenance.
- NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_assertion evidence source_evidence_literature NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_provenance.
- NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_provenance.