Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_assertion type Assertion NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_head.
- NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_provenance.
- NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_assertion evidence source_evidence_literature NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_provenance.
- NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_assertion SIO_000772 11257260 NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_provenance.
- NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_assertion wasDerivedFrom befree-20150227 NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_provenance.
- NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_assertion wasGeneratedBy ECO_0000203 NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_provenance.