Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_provenance.
- NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_assertion description "[Three patients showed extra copies of chromosome 21 including a case in which the trisomy 21 (+21) clone was distinct from the one harboring TEL/AML1 gene fusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_provenance.
- NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_assertion evidence source_evidence_literature NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_provenance.
- NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_assertion SIO_000772 11516105 NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_provenance.
- NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_assertion wasDerivedFrom befree-20150227 NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_provenance.
- NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_assertion wasGeneratedBy ECO_0000203 NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP387054.RAZN3kxmWbdv9cxeauHvP9O0xVagrsxCytTRniGcASSUc130_provenance.