Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_provenance.
- NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_assertion description "[The larger Type I deletions are flanked by BP1 and BP3 in both Prader-Willi and Angelman syndrome subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_provenance.
- NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_assertion evidence source_evidence_literature NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_provenance.
- NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_assertion SIO_000772 21359847 NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_provenance.
- NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_assertion wasDerivedFrom befree-20140225 NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_provenance.
- NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_assertion wasGeneratedBy ECO_0000203 NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP482290.RAya1L56Ukbbmk0W_yjadM3L7RRYVBouYFfGgiWznaepA130_provenance.