Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_provenance.
- NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_assertion description "[We have identified several recurrent regions of UPD and CNC in CML that may be of pathogenetic importance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_provenance.
- NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_assertion evidence source_evidence_literature NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_provenance.
- NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_assertion SIO_000772 20410925 NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_provenance.
- NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_assertion wasDerivedFrom befree-20140225 NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_provenance.
- NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_assertion wasGeneratedBy ECO_0000203 NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP218953.RAcv9Q7LVw6ovvcoeiIkpAGQTrgpD0trWh6X8nCD0vs1M130_provenance.