Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_assertion type Assertion NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_head.
- NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_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." NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_provenance.
- NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_assertion evidence source_evidence_literature NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_provenance.
- NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_assertion SIO_000772 19369868 NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_provenance.
- NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_assertion wasDerivedFrom befree-20150227 NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_provenance.
- NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_assertion wasGeneratedBy ECO_0000203 NP869689.RAYfOBrneoguhJmiPtRmj6U52_a2HTcHSYdmadhMQe6F4130_provenance.