Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_assertion> ?p ?o ?g. }
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- NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_assertion type Assertion NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_head.
- NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_assertion description "[Cystinuria is a primary inherited aminoaciduria caused by mutations in the genes that encode the two subunits (neutral and basic amino acid transport protein rBAT and b(0,+)-type amino acid transporter 1) of the amino acid transport system b(0,+).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_provenance.
- NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_assertion evidence source_evidence_literature NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_provenance.
- NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_assertion SIO_000772 20517292 NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_provenance.
- NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_assertion wasDerivedFrom befree-20150227 NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_provenance.
- NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_assertion wasGeneratedBy ECO_0000203 NP696360.RAfJ6cL-urQHVRoMVBWECx3LvpUFUXX_1nKqTx8MiS_vU130_provenance.