Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_assertion> ?p ?o ?g. }
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- NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_assertion type Assertion NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_head.
- NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_assertion description "[In our study we investigated the contribution of heterozygosity for common variations considered either potentially pathogenic or susceptibility alleles for cholesterol cholelithiasis in adults (c.523A>G (p.Thr175Ala) and c.1954A>G (p.Arg652Gly) in ABCB4, c.1331T>C (p.Val444Ala) in ABCB11 and c.55 G>C (p.Asp19His) in ABCG8) to the aetiology of paediatric idiopathic gallstone disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_provenance.
- NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_assertion evidence source_evidence_literature NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_provenance.
- NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_assertion SIO_000772 20163776 NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_provenance.
- NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_assertion wasDerivedFrom gad-20150221 NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_provenance.
- NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_assertion wasGeneratedBy ECO_0000203 NP164715.RALsfTgwLp_3JA1eIC0iYk9v2lCKM_Wv2qfC8Cy2npHQE130_provenance.