Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_assertion> ?p ?o ?g. }
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- NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_assertion type Assertion NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_head.
- NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_assertion description "[This study was designed to define the prevalence of CH due to mutations of PAX8, NKX2-1 [encoding thyroid transcription factor (TTF)-1], FOXE1 (encoding TTF-2), and NKX2-5 among patients with permanent primary CH and in the general population in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_provenance.
- NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_assertion evidence source_evidence_literature NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_provenance.
- NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_assertion SIO_000772 20157192 NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_provenance.
- NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_assertion wasDerivedFrom befree-20150227 NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_provenance.
- NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_assertion wasGeneratedBy ECO_0000203 NP333994.RAEkTKOIjQPdlWp64q9SpW60uja8Vf-97dTuHKjX4VPNc130_provenance.