Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_provenance.
- NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_assertion description "[AML1 point mutation is one of the major driving forces of myelodysplastic syndrome and acute myeloid leukemia, and these mutations may represent a distinct clinicopathologic-genetic entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_provenance.
- NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_assertion evidence source_evidence_literature NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_provenance.
- NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_assertion SIO_000772 14615365 NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_provenance.
- NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_assertion wasDerivedFrom lhgdn-20090331 NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_provenance.
- NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_assertion wasGeneratedBy ECO_0000203 NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP188235.RAvjfGddU4nhiaAxKd0Idr8WE0BNG0tJCXecnkIgGCi_E130_provenance.