Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_provenance.
- NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_assertion description "[Thus, GATA2 joins RUNX1 and CEBPA not only as a familial leukemia gene but also as a cause of a complex congenital immunodeficiency that evolves over decades and combines predisposition to infection and myeloid malignancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_provenance.
- NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_assertion evidence source_evidence_literature NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_provenance.
- NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_assertion SIO_000772 21670465 NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_provenance.
- NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_assertion wasDerivedFrom befree-20140225 NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_provenance.
- NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_assertion wasGeneratedBy ECO_0000203 NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_provenance.
- befree-20140225 importedOn "2014-02-25" NP817709.RAvVFx9ha39ISFXM9vx98ZZtTtfeiiuX3pnoZLr_ArOow130_provenance.