Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_provenance.
- NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_assertion description "[Germline GATA2 mutations are involved in a group of complex syndromes with overlapping clinical features of immune deficiency, lymphedema and propensity to acute myeloid leukemia or myelodysplastic syndrome (AML-MDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_provenance.
- NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_assertion evidence source_evidence_literature NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_provenance.
- NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_assertion SIO_000772 24754962 NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_provenance.
- NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_assertion wasDerivedFrom befree-2016 NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_provenance.
- NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_assertion wasGeneratedBy ECO_0000203 NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1175669.RAo18f0abOWjI2JrJMQz1krMcsWfztf7Q18LLAqHgdMuM130_provenance.