Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_provenance.
- NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_assertion description "[Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_provenance.
- NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_assertion evidence source_evidence_literature NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_provenance.
- NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_assertion SIO_000772 14740321 NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_provenance.
- NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_assertion wasDerivedFrom gad-20150221 NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_provenance.
- NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_assertion wasGeneratedBy ECO_0000203 NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_provenance.
- gad-20150221 importedOn "2015-02-21" NP69108.RAQGiatzKkYpyU_Zg-ROwRMFSqXpvGvAJXJmk9R_BRF8A130_provenance.