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- source_evidence_literature type ECO_0000212 NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- befree-20150227 importedOn "2015-02-27" NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_assertion wasGeneratedBy ECO_0000203 NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_assertion wasDerivedFrom befree-20150227 NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_assertion SIO_000772 11576738 NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_assertion evidence source_evidence_literature NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_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." NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.