Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_provenance.
- NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_assertion description "[Conventional chromosome analysis was obtained in 57 patients either at diagnosis or within 1 year of the array CGH study; all 21 patients with PV and 11 with ET displayed normal cytogenetic findings despite the presence of CNCs in 29% and 18%, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_provenance.
- NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_assertion evidence source_evidence_literature NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_provenance.
- NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_assertion SIO_000772 18937974 NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_provenance.
- NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_assertion wasDerivedFrom befree-20140225 NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_provenance.
- NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_assertion wasGeneratedBy ECO_0000203 NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP334162.RAqEocjWmuwVjL0Zio-F7t-iE_V6GtJfqpFEe3LWWIReo130_provenance.