Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion wasGeneratedBy ECO_0000203 NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion wasDerivedFrom lhgdn-20090331 NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion SIO_000772 18536571 NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion evidence source_evidence_literature NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion description "[REVIEW: Congenital neutropenia patients with acquired CSF3R mutations define a group with high risk for development of leukemia; discussion of possible pathomechanism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.