Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_provenance.
- NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_assertion description "[To identify acquired somatic mutations associated with myeloid transformation in patients with GATA2 mutations, we sequenced the region of the ASXL1 gene previously associated with transformation from myelodysplasia to myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_provenance.
- NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_assertion evidence source_evidence_literature NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_provenance.
- NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_assertion SIO_000772 24077845 NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_provenance.
- NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_assertion wasDerivedFrom befree-20150227 NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_provenance.
- NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_assertion wasGeneratedBy ECO_0000203 NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP418989.RAbv3KCeHfLfbnhmD0gV11xwFs-CeQ_NfQXqwZ0WkXwSU130_provenance.