Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1211303.RASv50ZmCEVa9Rsu-nLsCaa2qo4Ehu_b6LlNCNX9LwFgw130_provenance.