Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_provenance.
- NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_assertion description "[NUP98-HOXD13 transgenic mice develop a highly penetrant, severe myelodysplastic syndrome that progresses to acute leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_provenance.
- NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_assertion evidence source_evidence_literature NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_provenance.
- NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_assertion SIO_000772 15755899 NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_provenance.
- NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_assertion wasDerivedFrom befree-20140225 NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_provenance.
- NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_assertion wasGeneratedBy ECO_0000203 NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP490536.RAyYTwKNYmHVFcQovL12m2oMAw2zZthKd2ORleEoXjNMQ130_provenance.