Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_provenance.
- NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_assertion description "[hMICL and CD123 in combination with a CD45/CD34/CD117 backbone - a universal marker combination for the detection of minimal residual disease in acute myeloid leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_provenance.
- NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_assertion evidence source_evidence_literature NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_provenance.
- NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_assertion SIO_000772 24152218 NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_provenance.
- NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_assertion wasDerivedFrom befree-2016 NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_provenance.
- NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_assertion wasGeneratedBy ECO_0000203 NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1121878.RAspJFhpdH9YcfnS2Dr3gV8dlelLLE5OO9X-40D9c1KYw130_provenance.