Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_provenance.
- NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_assertion description "[However, IDH-mutated patients were more likely to be nullizygous for JAK2 46/1 haplotype, especially in PMF (P=0.04), and less likely to display complex karyotype, in blast-phase disease (P<0.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_provenance.
- NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_assertion evidence source_evidence_literature NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_provenance.
- NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_assertion SIO_000772 20508616 NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_provenance.
- NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_assertion wasDerivedFrom befree-20150227 NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_provenance.
- NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_assertion wasGeneratedBy ECO_0000203 NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP519121.RAWDXfR1bhAiiwE9AgpfCvMBGQd6hh-zdqkDhd2MgQyjQ130_provenance.