Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_assertion> ?p ?o ?g. }
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- NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_assertion type Assertion NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_head.
- NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_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." NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_provenance.
- NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_assertion evidence source_evidence_literature NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_provenance.
- NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_assertion SIO_000772 9649565 NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_provenance.
- NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_assertion wasDerivedFrom befree-20140225 NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_provenance.
- NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_assertion wasGeneratedBy ECO_0000203 NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_provenance.