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- NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_assertion type Assertion NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_head.
- NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_assertion wasGeneratedBy ECO_0000203 NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_provenance.
- NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_assertion wasDerivedFrom befree-2016 NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_provenance.
- NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_assertion SIO_000772 18726931 NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_provenance.
- NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_assertion evidence source_evidence_literature NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_provenance.
- NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_assertion description "[The FOXL2 gene is one of 10 forkhead genes, the mutations of which lead to human developmental disorders, often with ocular manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689656.RA3pjNxiXhWCp9wTht-kXG-WnpNrSpW_NK6ZU7o42n2Vk130_provenance.