Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_assertion> ?p ?o ?g. }
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- NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_assertion type Assertion NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_head.
- NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_assertion description "[Argininemia is an autosomal recessive disorder caused by a deficiency in the liver-type arginase enzyme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_provenance.
- NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_assertion evidence source_evidence_literature NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_provenance.
- NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_assertion SIO_000772 7649538 NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_provenance.
- NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_assertion wasDerivedFrom befree-2016 NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_provenance.
- NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_assertion wasGeneratedBy ECO_0000203 NP1316491.RAKaR3nghRDrDzywWb1XXnhp2-ISMTjxcO_7g4jHfyfLE130_provenance.