Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP242484.RASV5NNjPvGd9sY7OfOe5I7PHgSr3D0fvTIkCX09ZuXII130_assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP242484.RASV5NNjPvGd9sY7OfOe5I7PHgSr3D0fvTIkCX09ZuXII130_provenance.
• NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance.
• assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP699621.RAdFeZQ9Ps_T786B9HcnOkn6WEegbmTCWgcHCh25mV0gI130_assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699621.RAdFeZQ9Ps_T786B9HcnOkn6WEegbmTCWgcHCh25mV0gI130_provenance.
• assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP699650.RAqvwQCz99ILbzTkWCGuriBBuznkEqkA2O7PNWq-62HAo130_assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699650.RAqvwQCz99ILbzTkWCGuriBBuznkEqkA2O7PNWq-62HAo130_provenance.
• NP871404.RATeNpBsb3TN-Jr3sI64ATIxAKb8mdCC1aoJGwHt2OPZo130_assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871404.RATeNpBsb3TN-Jr3sI64ATIxAKb8mdCC1aoJGwHt2OPZo130_provenance.
• NP871405.RAWiOiEmBMa8qmUMakH4UhZqgjTqT30zBmaB_2NOJWfmo130_assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871405.RAWiOiEmBMa8qmUMakH4UhZqgjTqT30zBmaB_2NOJWfmo130_provenance.
• NP699643.RA0Yy7ZB-llAmpMNpUtKqDpAZL9wbdD6MX3utCFg9Uii0130_assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699643.RA0Yy7ZB-llAmpMNpUtKqDpAZL9wbdD6MX3utCFg9Uii0130_provenance.
• NP871406.RAK6h9q03-mjglZfnDLPdBHyWjNedHVJgT6de-muQkdac130_assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871406.RAK6h9q03-mjglZfnDLPdBHyWjNedHVJgT6de-muQkdac130_provenance.