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- source_evidence_literature type ECO_0000212 NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_provenance.
- NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_assertion description "[The Seipin/BSCL2 gene was originally identified as a loss-of-function gene for congenital generalized lipodystrophy type 2 (CGL2), a condition characterized by severe lipoatrophy, insulin resistance, hypertriglyceridaemia and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_provenance.
- NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_assertion evidence source_evidence_literature NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_provenance.
- NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_assertion SIO_000772 18790819 NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_provenance.
- NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_assertion wasDerivedFrom befree-2016 NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_provenance.
- NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_assertion wasGeneratedBy ECO_0000203 NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_provenance.
- befree-2016 importedOn "2016-02-19" NP692963.RAae9YupH1ZMkjtuAUY0Lc5m9wyKlF-p_4YjF74q2rPfI130_provenance.