Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_assertion> ?p ?o ?g. }
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- NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_assertion type Assertion NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_head.
- NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_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." NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_provenance.
- NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_assertion evidence source_evidence_literature NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_provenance.
- NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_assertion SIO_000772 21437635 NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_provenance.
- NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_assertion wasDerivedFrom befree-20140225 NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_provenance.
- NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_assertion wasGeneratedBy ECO_0000203 NP212111.RAfKqa60eAIlS_EoEjGJecsCX-d-XQ2PFPxGsucOjHxTU130_provenance.