Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_provenance.
- NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_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." NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_provenance.
- NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_assertion evidence source_evidence_literature NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_provenance.
- NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_assertion SIO_000772 11257260 NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_provenance.
- NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_assertion wasDerivedFrom befree-20140225 NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_provenance.
- NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_assertion wasGeneratedBy ECO_0000203 NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP515217.RAon0rhuNansxE91iyr-uW1SmnVW4FhjxS9OwZqrIuYQ0130_provenance.