Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_provenance.
- NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_assertion description "[We sequenced the translocation breakpoints of 56 patients with childhood ALL or AML harboring t(12;21), t(8;21), t(15;17), inv(16), and t(1;19), and demonstrated, with the notable exception of t(1;19), that these rearrangements are commonly detected in the neonatal blood spots (Guthrie cards) of the cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_provenance.
- NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_assertion evidence source_evidence_literature NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_provenance.
- NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_assertion SIO_000772 15967214 NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_provenance.
- NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_assertion wasDerivedFrom befree-20150227 NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_provenance.
- NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_assertion wasGeneratedBy ECO_0000203 NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP289470.RAxACM1VrTREx2DdpMn7GVFSyj769dn05pT-NWQyvJ93k130_provenance.