Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_assertion> ?p ?o ?g. }
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- NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_assertion type Assertion NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_head.
- NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_assertion description "[Mutations in paired box gene 6 (PAX6) are the major cause of aniridia that may be associated with several other developmental anomalies of the eye, including microcornea in rare cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_provenance.
- NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_assertion evidence source_evidence_literature NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_provenance.
- NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_assertion SIO_000772 25189681 NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_provenance.
- NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_assertion wasDerivedFrom befree-2016 NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_provenance.
- NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_assertion wasGeneratedBy ECO_0000203 NP1216990.RA9mzvEw0nzxFOi7W-dVgC3d6c3SyQYq0Q4MFvYNAXMiw130_provenance.