Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance.
- NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_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." NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance.
- NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_assertion evidence source_evidence_literature NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance.
- NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_assertion SIO_000772 9649565 NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance.
- NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_assertion wasDerivedFrom befree-20150227 NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance.
- NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_assertion wasGeneratedBy ECO_0000203 NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance.