Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_assertion> ?p ?o ?g. }
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- NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_assertion type Assertion NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_head.
- NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_assertion description "[Taken together, this report further suggests that hereditary 5-oxoprolinase deficiency is a benign biochemical condition caused by mutations in the OPLAH gene, which are transmitted in an autosomal recessive manner, but 5-oxoprolinuria may be a chance association in other disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance.
- NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_assertion evidence source_evidence_literature NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance.
- NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_assertion SIO_000772 25129617 NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance.
- NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_assertion wasDerivedFrom befree-2016 NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance.
- NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_assertion wasGeneratedBy ECO_0000203 NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance.