Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_provenance.
- NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_assertion description "[Mutation analysis of ATP13A2 gene in Chinese patients with familial autosomal recessive early-onset parkinsonism]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_provenance.
- NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_assertion evidence source_evidence_literature NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_provenance.
- NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_assertion SIO_000772 19806583 NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_provenance.
- NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_assertion wasDerivedFrom gad-20150221 NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_provenance.
- NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_assertion wasGeneratedBy ECO_0000203 NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_provenance.
- gad-20150221 importedOn "2015-02-21" NP157584.RAGsXbBdjqrYHAm54zVqgbe90vOdCAH4dhOtMqsfO0m5c130_provenance.