Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_provenance.
- NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_assertion description "[First, we found that absence of SOX2 in the developing Rathke pouch of conditional embryos led to severe anterior lobe hypoplasia with drastically reduced expression of the pituitary-specific transcription factor POU class 1 homeobox 1 (POU1F1) as well as severe disruption of somatotroph and thyrotroph differentiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_provenance.
- NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_assertion evidence source_evidence_literature NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_provenance.
- NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_assertion SIO_000772 22945632 NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_provenance.
- NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_assertion wasDerivedFrom befree-2016 NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_provenance.
- NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_assertion wasGeneratedBy ECO_0000203 NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1010056.RAid505MZJ0Uv0uhaG8gEA3JVTyI_B4qXCocrSMrdLRZU130_provenance.