Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_provenance.
- NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_assertion description "[FISH with the probe generated from the hsr of GR also painted the hsr in MLS/P, indicating that the two hsrs have shared homology, which indicates that the amplification of 8q24/C-MYC as the origin of hsr may be a nonrandom genomic alteration in ovc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_provenance.
- NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_assertion evidence source_evidence_literature NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_provenance.
- NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_assertion SIO_000772 10549271 NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_provenance.
- NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_assertion wasDerivedFrom befree-20140225 NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_provenance.
- NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_assertion wasGeneratedBy ECO_0000203 NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP935061.RAD6YuUkMy3VAnqppdiikXJzgRnQke1edB1XVkK0tHSp0130_provenance.