Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_provenance.
- NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_assertion description "[The patient is examined in light of other reported patients with deletions and/or translocations involving the regions between 11p12 --> 11p14 including patients with WAGR + obesity (WAGRO) as well as with other reported patients with aniridia and congenital ptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_provenance.
- NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_assertion evidence source_evidence_literature NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_provenance.
- NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_assertion SIO_000772 16646034 NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_provenance.
- NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_assertion wasDerivedFrom befree-2016 NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_provenance.
- NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_assertion wasGeneratedBy ECO_0000203 NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_provenance.
- befree-2016 importedOn "2016-02-19" NP547349.RAjP7sullZmWFmYzf0OT5-Yb9ElGyql2hd9r_ogwsCFK8130_provenance.