Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_provenance.
- NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_assertion description "[Primary hyperoxaluria type II (PH2) is a rare monogenic disorder that is characterized by a lack of the enzyme that catalyzes the reduction of hydroxypyruvate to D-glycerate, the reduction of glyoxylate to glycolate and the oxidation of D-glycerate to hydroxypyruvate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_provenance.
- NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_assertion evidence source_evidence_literature NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_provenance.
- NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_assertion SIO_000772 10484776 NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_provenance.
- NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_assertion wasDerivedFrom befree-2016 NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_provenance.
- NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_assertion wasGeneratedBy ECO_0000203 NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_provenance.
- befree-2016 importedOn "2016-02-19" NP262853.RAQxlP_t4Oa1t3QqiiLv6SIQfkpXXJwLV4O59gx9TwDXc130_provenance.