Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_assertion> ?p ?o ?g. }
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- NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_assertion type Assertion NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_head.
- NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_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." NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_provenance.
- NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_assertion evidence source_evidence_literature NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_provenance.
- NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_assertion SIO_000772 11528503 NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_provenance.
- NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_assertion wasDerivedFrom befree-20140225 NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_provenance.
- NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_assertion wasGeneratedBy ECO_0000203 NP637848.RAAdAQLxsiYx4b1QKhKBxA4mQt4ZzgsQ_fMcrDsUSVdbo130_provenance.