Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP240547.RAZDw50B7cjmNdpcz-6-GnWqOGOaT0bKe-NEa_3xjobUU130_provenance.