Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion description "[A wide spectrum of genetic aberrations has been associated with MDS, including chromosomal translocations involving the NUP98 gene, most commonly leading to fusions of NUP98 with abd-b group HOX genes, including HOXD13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion evidence source_evidence_literature NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion SIO_000772 18648006 NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion wasDerivedFrom befree-20140225 NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion wasGeneratedBy ECO_0000203 NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- befree-20140225 importedOn "2014-02-25" NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.