Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_provenance.
- NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_assertion description "[A significantly lower expression of LAIR1 was observed in patients with Binet stage B or C disease (P=0.023), and in the presence of high-risk cytogenetic abnormalities (P=0.048) or unmutated immunoglobulin heavy chain variable region genes (P<0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_provenance.
- NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_assertion evidence source_evidence_literature NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_provenance.
- NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_assertion SIO_000772 24415628 NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_provenance.
- NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_assertion wasDerivedFrom befree-2016 NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_provenance.
- NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_assertion wasGeneratedBy ECO_0000203 NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1144283.RADP41tOLkEaZCHINoKv5cRG3YRZUbl8_mCNjEa3k8BOM130_provenance.