Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_provenance.
- NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_assertion description "[Two hereditary human leukemia syndromes are severe congenital neutropenia (SCN), caused by mutations in the gene ELA2, encoding the protease neutrophil elastase, and familial platelet disorder with acute myelogenous leukemia (AML), caused by mutations in the gene AML1, encoding the transcription factor core-binding factor alpha (CBFalpha).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_provenance.
- NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_assertion evidence source_evidence_literature NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_provenance.
- NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_assertion SIO_000772 14594802 NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_provenance.
- NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_assertion wasDerivedFrom befree-20140225 NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_provenance.
- NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_assertion wasGeneratedBy ECO_0000203 NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP444711.RAOzzkOdzqJAZPK0e8ao2XSYSqFHIcoklQTrwa06SQLfA130_provenance.