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- NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_assertion type Assertion NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_head.
- 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.
- NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_assertion evidence source_evidence_literature NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_provenance.
- NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_assertion SIO_000772 19369868 NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_provenance.
- NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_assertion wasDerivedFrom befree-20140225 NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_provenance.
- NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_assertion wasGeneratedBy ECO_0000203 NP879932.RA5xc_GYXv_o27rodG41xKnrjjdIRo5QqCAe4IDdwyXME130_provenance.