Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_assertion> ?p ?o ?g. }
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- NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_assertion type Assertion NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_head.
- NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_assertion description "[Recent studies have implicated mutations in the ATP-binding cassette transporter A1, ABCA1, as a cause of Tangier disease (TD) and familial hypoalphalipoproteinemia (FHA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_provenance.
- NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_assertion evidence source_evidence_literature NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_provenance.
- NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_assertion SIO_000772 14576201 NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_provenance.
- NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_assertion wasDerivedFrom befree-20150227 NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_provenance.
- NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_assertion wasGeneratedBy ECO_0000203 NP218575.RAquBgkceIrtFxI72_0Tlio4gKBsZULf4DaoR3TfS4oZI130_provenance.