Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_assertion> ?p ?o ?g. }
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- NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_assertion type Assertion NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_head.
- NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_assertion description "[Alpha-1-antitrypsin (A1AT) deficiency is the most common genetic cause of liver disease in children; however, the role of polymorphic heterogeneity in the A1AT gene as a modifier of other forms of pediatric liver disease is not clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_provenance.
- NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_assertion evidence source_evidence_literature NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_provenance.
- NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_assertion SIO_000772 17204961 NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_provenance.
- NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_assertion wasDerivedFrom gad-20150221 NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_provenance.
- NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_assertion wasGeneratedBy ECO_0000203 NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_provenance.