Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance.