Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_provenance.
- NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_assertion description "[A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_provenance.
- NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_assertion evidence source_evidence_literature NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_provenance.
- NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_assertion SIO_000772 18445675 NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_provenance.
- NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_assertion wasDerivedFrom befree-2016 NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_provenance.
- NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_assertion wasGeneratedBy ECO_0000203 NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_provenance.
- befree-2016 importedOn "2016-02-19" NP668514.RAA6V0uFE0tPigdii55zthJpHObQAPY8pYuosm9PKuCio130_provenance.