Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_provenance.
- NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_assertion description "[PHD1 is encoded by an alternatively spliced exon that is occasionally deleted in T-cell leukemia, and its absence produces an MLL mutant protein that is deficient for holocomplex formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_provenance.
- NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_assertion evidence source_evidence_literature NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_provenance.
- NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_assertion SIO_000772 21670200 NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_provenance.
- NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_assertion wasDerivedFrom befree-20150227 NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_provenance.
- NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_assertion wasGeneratedBy ECO_0000203 NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP963371.RA9lUUOjwAnEcPpZl5ia6PVLRJK0QGmSq7NuKlUK3PZKk130_provenance.