Matches in Nanopublications for { ?s ?p "[Recent studies have identified mutations that cause lipin-1 or lipin-2 deficiency in humans, leading to acute myoglobinuria in childhood or the inflammatory disorder Majeed syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_assertion description "[Recent studies have identified mutations that cause lipin-1 or lipin-2 deficiency in humans, leading to acute myoglobinuria in childhood or the inflammatory disorder Majeed syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_provenance.
- NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_assertion description "[Recent studies have identified mutations that cause lipin-1 or lipin-2 deficiency in humans, leading to acute myoglobinuria in childhood or the inflammatory disorder Majeed syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_provenance.
- NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_assertion description "[Recent studies have identified mutations that cause lipin-1 or lipin-2 deficiency in humans, leading to acute myoglobinuria in childhood or the inflammatory disorder Majeed syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_provenance.
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- assertion description "[Recent studies have identified mutations that cause lipin-1 or lipin-2 deficiency in humans, leading to acute myoglobinuria in childhood or the inflammatory disorder Majeed syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
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- NP732624.RAl7hRoH98EMjGMO9kBfXYLmjwQ2-3mhOsqtOQXFrohNk130_assertion description "[Recent studies have identified mutations that cause lipin-1 or lipin-2 deficiency in humans, leading to acute myoglobinuria in childhood or the inflammatory disorder Majeed syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP732624.RAl7hRoH98EMjGMO9kBfXYLmjwQ2-3mhOsqtOQXFrohNk130_provenance.
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