Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_assertion type Assertion NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_head.
- 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.
- NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_assertion evidence source_evidence_literature NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_provenance.
- NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_assertion SIO_000772 19369868 NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_provenance.
- NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_assertion wasDerivedFrom befree-20140225 NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_provenance.
- NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_assertion wasGeneratedBy ECO_0000203 NP201082.RA7czRY_to3ObXoQT50zlXbEwIX-T7GNotFJYFOCIBjHU130_provenance.