Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_provenance.
- NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_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." NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_provenance.
- NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_assertion evidence source_evidence_literature NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_provenance.
- NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_assertion SIO_000772 20508616 NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_provenance.
- NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_assertion wasDerivedFrom befree-20140225 NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_provenance.
- NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_assertion wasGeneratedBy ECO_0000203 NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP814321.RAajUIZnaBNd-5A7aoY3QT5-ngJGMgnGJXTDtDAhRKk5s130_provenance.