Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_provenance.
- NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_assertion description "[The underlying genetic defect for most cases of RD was recently identified in the gene encoding adenylate kinase 2 (AK2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_provenance.
- NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_assertion evidence source_evidence_literature NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_provenance.
- NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_assertion SIO_000772 19896777 NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_provenance.
- NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_assertion wasDerivedFrom befree-20140225 NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_provenance.
- NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_assertion wasGeneratedBy ECO_0000203 NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP853880.RADV8-PQAmnlwN3_wfHP3FlfEFU4FICSRDPQZ7KGGzi_I130_provenance.