Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_assertion> ?p ?o ?g. }
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- NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_assertion type Assertion NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_head.
- NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_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." NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_provenance.
- NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_assertion evidence source_evidence_literature NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_provenance.
- NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_assertion SIO_000772 12812307 NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_provenance.
- NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_assertion wasDerivedFrom befree-20140225 NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_provenance.
- NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_assertion wasGeneratedBy ECO_0000203 NP776118.RAg02glcgN5mEwsx9JQjslVoNH61VfWFLC20gg8JCRuOw130_provenance.