Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_assertion> ?p ?o ?g. }
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- NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_assertion type Assertion NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_head.
- NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_assertion wasGeneratedBy ECO_0000203 NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_provenance.
- NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_assertion wasDerivedFrom befree-2016 NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_provenance.
- NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_assertion SIO_000772 21428921 NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_provenance.
- NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_assertion evidence source_evidence_literature NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_provenance.
- NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_assertion description "[Mutations in genes encoding either hamartin [TSC1 (tuberous sclerosis complex 1)] or tuberin (TSC2) result in a multisystem disorder characterized by the development of benign tumours and hamartomas in several organs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881660.RA3TbFMF8eMOYZhuDxljmu33SFzGiz3fVsGcOc93_ItXc130_provenance.