Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_provenance.
- NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_assertion description "[Erythrocyte (RBC) protein 4.2 (P4.2)-deficiency observed in Japanese individuals results in a hemolytic anemia associated with abnormally shaped (spherocytic, ovalocytic, and elliptocytic), osmotically fragile RBCs, the clinical presentation of which resembles hereditary spherocytosis (HS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_provenance.
- NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_assertion evidence source_evidence_literature NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_provenance.
- NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_assertion SIO_000772 1558976 NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_provenance.
- NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_assertion wasDerivedFrom befree-20140225 NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_provenance.
- NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_assertion wasGeneratedBy ECO_0000203 NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP835927.RA6pR4gkVLodIbDjRhgBarYzbd25GZ2mDJ6P8UCE2F6-s130_provenance.