Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_assertion> ?p ?o ?g. }
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- NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_assertion type Assertion NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_head.
- NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_assertion description "[Axenfeld-Rieger ocular dysgenesis is associated with mutations of the human PITX2 and FOXC1 genes, which encode transcription factors of the homeodomain and forkhead types, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_provenance.
- NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_assertion evidence source_evidence_literature NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_provenance.
- NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_assertion SIO_000772 16449236 NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_provenance.
- NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_assertion wasDerivedFrom befree-20140225 NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_provenance.
- NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_assertion wasGeneratedBy ECO_0000203 NP651912.RAIOkkc6V3As5m4Hc6djHLLjaNSvSlczWi7jsacowfnoo130_provenance.