Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_provenance.
- NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_assertion description "[We genotyped the EPO rS1617640 SNP in 189 patients with MDS, 257 with acute myeloid leukemia (AML), 106 with acute lymphoblastic leukemia, 97 with chronic lymphocytic leukemia, 353 with chronic myeloid leukemia, and 95 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_provenance.
- NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_assertion evidence source_evidence_literature NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_provenance.
- NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_assertion SIO_000772 21078205 NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_provenance.
- NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_assertion wasDerivedFrom gad-20150221 NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_provenance.
- NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_assertion wasGeneratedBy ECO_0000203 NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP188322.RAgp7HspzBlJe2rmRvFc47nAcmEVjc9H13AelzsVAzWZQ130_provenance.