Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_provenance.
- NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_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." NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_provenance.
- NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_assertion evidence source_evidence_literature NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_provenance.
- NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_assertion SIO_000772 21670465 NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_provenance.
- NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_assertion wasDerivedFrom befree-2016 NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_provenance.
- NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_assertion wasGeneratedBy ECO_0000203 NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_provenance.
- befree-2016 importedOn "2016-02-19" NP901708.RAQ3MJJLHMk6P9219lXTBm5DUlLd6iLHN0LxwFydpJb0c130_provenance.