Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_provenance.
- NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_assertion description "[To clarify some characteristics of phosphatidylinositol glycan-class A gene (PIG-A) mutations in aplastic anemia (AA) and myelodysplastic syndrome (MDS) patients compared with those in paroxysmal nocturnal hemoglobinuria (PNH) patients, we investigated PIG-A mutations in CD59- granulocytes and CD48- monocytes from seven AA, eight MDS, and 11 PNH Japanese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_provenance.
- NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_assertion evidence source_evidence_literature NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_provenance.
- NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_assertion SIO_000772 16467865 NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_provenance.
- NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_assertion wasDerivedFrom befree-20140225 NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_provenance.
- NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_assertion wasGeneratedBy ECO_0000203 NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP492324.RAObiN98uIwTGiRiflmTq9Po5VrPgs6PslCGWaur4yki8130_provenance.