Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance.
- NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_assertion description "[Primary familial and congenital polycythemia (PFCP or familial erythrocytosis) is a rare proliferative disorder of erythroid progenitor cells, characterized by elevated erythrocyte mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to erythropoietin (EPO), and autosomal dominant inheritance or sporadic occurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance.
- NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_assertion evidence source_evidence_literature NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance.
- NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_assertion SIO_000772 9649565 NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance.
- NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_assertion wasDerivedFrom befree-20140225 NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance.
- NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_assertion wasGeneratedBy ECO_0000203 NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance.