Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_provenance.
- NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_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." NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_provenance.
- NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_assertion evidence source_evidence_literature NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_provenance.
- NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_assertion SIO_000772 16467865 NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_provenance.
- NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_assertion wasDerivedFrom befree-20150227 NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_provenance.
- NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_assertion wasGeneratedBy ECO_0000203 NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP296791.RAOZn_GMHkJ5ffS1q6ecA1r21ChbeISQHgfWApl68dimQ130_provenance.