Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_provenance.
- NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_assertion description "[We report a patient with myelodysplastic syndrome (refractory anemia) showing the karyotype 46,XY,+1,der(1;10)(q10;p10), resulting in trisomy 1q and monosomy 10q abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_provenance.
- NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_assertion evidence source_evidence_literature NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_provenance.
- NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_assertion SIO_000772 17213027 NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_provenance.
- NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_assertion wasDerivedFrom befree-20140225 NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_provenance.
- NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_assertion wasGeneratedBy ECO_0000203 NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP350307.RA5B9BqtV5bztkjUH--B46nY6PSw6weZ2e62SMIx6k8Vc130_provenance.