Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_provenance.
- NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_assertion description "[Although heterozygosity for cystathionine beta-synthase (CBS) deficiency has been excluded as a major genetic cause of mild hyperhomocysteinaemia in vascular disease, mutations in (non-)coding DNA sequences may lead to a mildly decreased CBS expression and, consequently, to elevated plasma homocysteine levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_provenance.
- NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_assertion evidence source_evidence_literature NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_provenance.
- NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_assertion SIO_000772 11528503 NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_provenance.
- NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_assertion wasDerivedFrom befree-20150227 NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_provenance.
- NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_assertion wasGeneratedBy ECO_0000203 NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1018382.RAjqXmzv-a9Iona05n6-d7PQ4j9bQxWA_t8WoUUd9VBKs130_provenance.