Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_provenance.
- NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_assertion wasGeneratedBy ECO_0000203 NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_provenance.
- NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_assertion wasDerivedFrom befree-20140225 NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_provenance.
- NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_assertion SIO_000772 11576738 NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_provenance.
- NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_assertion evidence source_evidence_literature NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_provenance.
- NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_assertion description "[PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP428267.RAQ3WRt8ySkypr249LnoMu7zOGYRS5NrqRHBw4nTXN35o130_provenance.