Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_assertion> ?p ?o ?g. }
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- NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_assertion type Assertion NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_head.
- NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_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." NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_provenance.
- NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_assertion evidence source_evidence_literature NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_provenance.
- NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_assertion SIO_000772 18790819 NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_provenance.
- NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_assertion wasDerivedFrom befree-20140225 NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_provenance.
- NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_assertion wasGeneratedBy ECO_0000203 NP899495.RAaRfm3khBszkTtZPS-jfUzRC7vf1ouN19-l140rz6eWg130_provenance.