Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_provenance.
- NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_assertion description "[In addition, FISH, with probes at D15S11 and GABR beta 3 from the Prader-Willi syndrome/Angelman's syndrome region, was performed on a subset of 25 of these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_provenance.
- NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_assertion evidence source_evidence_literature NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_provenance.
- NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_assertion SIO_000772 7618904 NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_provenance.
- NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_assertion wasDerivedFrom befree-20140225 NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_provenance.
- NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_assertion wasGeneratedBy ECO_0000203 NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP666139.RAqdeKPy8YR_fSwMlNMFOA5cJL_iee6-10VJlWelPnOBE130_provenance.