Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_provenance.
- NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_assertion description "[Cytomorphological alterations in peripheral blood films as well as bone marrow aspirates and histological findings in trephine biopsies result from cytogenetic and molecular abnormalities, epigenetic dysregulation and immune dysfunction and are key elements for setting the diagnosis of MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_provenance.
- NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_assertion evidence source_evidence_literature NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_provenance.
- NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_assertion SIO_000772 24507811 NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_provenance.
- NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_assertion wasDerivedFrom befree-20150227 NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_provenance.
- NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_assertion wasGeneratedBy ECO_0000203 NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781363.RAIOdd1QG4m1EAXYZWj06vI_cnqivDwl2kzcRcEhrxApY130_provenance.