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- source_evidence_literature type ECO_0000212 NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_provenance.