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- source_evidence_literature type ECO_0000212 NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_provenance.
- NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_assertion description "[Of the 17 individuals with ET, six (35%) had the JAK2 V617F mutation and one (6%) was found to have the MPL W515L mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_provenance.
- NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_assertion evidence source_evidence_literature NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_provenance.
- NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_assertion SIO_000772 19843380 NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_provenance.
- NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_assertion wasDerivedFrom befree-2016 NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_provenance.
- NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_assertion wasGeneratedBy ECO_0000203 NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_provenance.
- befree-2016 importedOn "2016-02-19" NP770416.RA805DYn3pRYoQqricj7NipdGo4BqcxnHyyIeVwOOSFwc130_provenance.