Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance.
- NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_assertion wasGeneratedBy ECO_0000203 NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance.
- NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_assertion wasDerivedFrom befree-20150227 NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance.
- NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_assertion SIO_000772 24297870 NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance.
- NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_assertion evidence source_evidence_literature NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance.
- NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_assertion description "[RUNX1 and NF-E2 overexpression was not detected in patients with EPO receptor (EPOR) gain-of-function, suggesting distinct mechanisms by which erythroid progenitors in polycythemias with defects of hypoxia sensing and EPOR mutations exert their EPO hypersensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378032.RAyVnw9wm3uwKr3nVf_5fFsB4pOjZtun0s69Nmb7kuhA4130_provenance.