Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_assertion type Assertion NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_head.
- NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_assertion description "[A cohort of 84 familial congenital or juvenile cataract index cases was screened for mutations in the EPHA2 gene by direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_provenance.
- NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_assertion evidence source_evidence_literature NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_provenance.
- NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_assertion SIO_000772 24014202 NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_provenance.
- NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_assertion wasDerivedFrom befree-2016 NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_provenance.
- NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_assertion wasGeneratedBy ECO_0000203 NP1108538.RAv1krw6A5Ouxu248Ai_NvEgKNTH7jX95BMz7m80d3c8k130_provenance.