Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_assertion> ?p ?o ?g. }
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- NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_assertion type Assertion NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_head.
- NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_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." NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance.
- NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_assertion evidence source_evidence_literature NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance.
- NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_assertion SIO_000772 9649565 NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance.
- NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_assertion wasDerivedFrom befree-2016 NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance.
- NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_assertion wasGeneratedBy ECO_0000203 NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance.