Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_provenance.
- NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_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." NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_provenance.
- NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_assertion evidence source_evidence_literature NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_provenance.
- NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_assertion SIO_000772 10396622 NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_provenance.
- NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_assertion wasDerivedFrom befree-2016 NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_provenance.
- NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_assertion wasGeneratedBy ECO_0000203 NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_provenance.
- befree-2016 importedOn "2016-02-19" NP256825.RAEgWMuAiOrVZTPSH2L1Ud9Wyfh2DTN9sAeT9VEnXe-YM130_provenance.