Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_assertion> ?p ?o ?g. }
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- NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_assertion type Assertion NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_head.
- NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_assertion description "[More recently mutations in the HESX1, the LHX3 and LHX4 transcription factor genes have also been described as a cause in patients with CPHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_provenance.
- NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_assertion evidence source_evidence_literature NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_provenance.
- NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_assertion SIO_000772 12812307 NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_provenance.
- NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_assertion wasDerivedFrom befree-2016 NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_provenance.
- NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_assertion wasGeneratedBy ECO_0000203 NP398554.RAiSTcYe-YQEDFLmoi7_iAZwOqCxNltZv3e2hED-VTgCY130_provenance.