Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_provenance.
- NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_assertion description "[X-chromosome DNA probes for the phosphoglycerate kinase (PGK) and hypoxanthine phosphoribosyl transferase (HPRT) genes were used to study clonality in haemopoietic cells from 63 women with myeloproliferative disease, idiopathic erythrocytosis, secondary erythrocytosis or normal red cell volumes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_provenance.
- NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_assertion evidence source_evidence_literature NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_provenance.
- NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_assertion SIO_000772 2775657 NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_provenance.
- NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_assertion wasDerivedFrom befree-2016 NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_provenance.
- NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_assertion wasGeneratedBy ECO_0000203 NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1296710.RAEfjk8a3MCQutgSkutUQr3O6Eu6MFeZ2dAaD4weiJYmM130_provenance.