Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_provenance.
- NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_assertion description "[Amplifying a polymorphic portion of the X chromosome-linked phosphoglycerate kinase (PGK) gene after selective digestion of the active X chromosome with a methylation-sensitive restriction enzyme gave results fully concordant with standard Southern blotting of DNA samples from normal (polyclonal) polymorphonuclear cells (PMN) as well as clonal PMN from patients with myelodysplastic syndrome and polycythemia vera (PCV).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_provenance.
- NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_assertion evidence source_evidence_literature NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_provenance.
- NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_assertion SIO_000772 1862109 NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_provenance.
- NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_assertion wasDerivedFrom befree-2016 NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_provenance.
- NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_assertion wasGeneratedBy ECO_0000203 NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP681691.RAl_n9lDAmOqWvLsimqAEmb8ep0tR634OFU3N8z_wfaoQ130_provenance.