Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_assertion> ?p ?o ?g. }
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- NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_assertion type Assertion NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_head.
- NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_assertion description "[Primary familial and congenital polycythaemia (PFCP) is a rare form of inherited erythrocytosis caused by heterozygous mutations in the erythropoietin receptor gene (EPOR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_provenance.
- NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_assertion evidence source_evidence_literature NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_provenance.
- NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_assertion SIO_000772 21437635 NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_provenance.
- NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_assertion wasDerivedFrom befree-20140225 NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_provenance.
- NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_assertion wasGeneratedBy ECO_0000203 NP868503.RAad81TH0Y_YGXoVYXP5UUSxKjV4iRFQhitpoxuxwAT6U130_provenance.