Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_provenance.
- NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_assertion description "[Recently, mutations in a novel gene, PINK1, encoding a 581 amino acid protein with both mitochondrial targeting and serine/threonine kinase domains, were identified as a cause of autosomal recessive parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_provenance.
- NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_assertion evidence source_evidence_literature NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_provenance.
- NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_assertion SIO_000772 16702191 NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_provenance.
- NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_assertion wasDerivedFrom befree-20140225 NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_provenance.
- NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_assertion wasGeneratedBy ECO_0000203 NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_provenance.
- befree-20140225 importedOn "2014-02-25" NP902348.RADpedyPrxun3ZR5-ykiOyMiBrnrVpOLMz4JaUFq2mp64130_provenance.