Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_assertion> ?p ?o ?g. }
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- NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_assertion type Assertion NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_head.
- NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_provenance.
- NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_assertion evidence source_evidence_literature NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_provenance.
- NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_assertion SIO_000772 21862621 NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_provenance.
- NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_assertion wasDerivedFrom befree-2016 NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_provenance.
- NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_assertion wasGeneratedBy ECO_0000203 NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_provenance.