Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_assertion> ?p ?o ?g. }
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- NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_assertion type Assertion NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_head.
- NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_assertion description "[Mutations in ABCR are associated with at least four inherited retinal dystrophies: Stargardt disease, Fundus Flavimaculatus, cone-rod dystrophy, and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_provenance.
- NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_assertion evidence source_evidence_literature NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_provenance.
- NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_assertion SIO_000772 10396622 NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_provenance.
- NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_assertion wasDerivedFrom befree-20140225 NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_provenance.
- NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_assertion wasGeneratedBy ECO_0000203 NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_provenance.