Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_provenance.
- NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_assertion description "[Overall, the incidence of the JAK2 V617F mutation was 87% in PV, 67% in ET, and 66% in CIM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_provenance.
- NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_assertion evidence source_evidence_literature NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_provenance.
- NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_assertion SIO_000772 16949922 NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_provenance.
- NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_assertion wasDerivedFrom befree-2016 NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_provenance.
- NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_assertion wasGeneratedBy ECO_0000203 NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_provenance.
- befree-2016 importedOn "2016-02-19" NP567273.RA_PU3kCPG5ULMJCzK1PSRCdGhlOW-PNlrpfQ15q73SQg130_provenance.