Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion> ?p ?o ?g. }
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- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion type Assertion NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_head.
- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion description "[Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion evidence source_evidence_literature NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion SIO_000772 19279310 NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion wasDerivedFrom befree-20150227 NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.
- NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_assertion wasGeneratedBy ECO_0000203 NP404455.RA-pILQTUfbJMbDCQ7g5S4ZEv8x_UsT2a72eqhrHzBlNk130_provenance.