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- source_evidence_literature type ECO_0000212 NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_provenance.
- NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_assertion description "[Mutations in the ATP-binding cassette transporter ABCA1 underlie Tangier disease and familial hypoalphaliproteinemia (FHA), disorders that are characterised by reduced high-density lipoprotein-cholesterol (HDL-C) concentration and cholesterol efflux, and increased coronary artery disease (CAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_provenance.
- NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_assertion evidence source_evidence_literature NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_provenance.
- NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_assertion SIO_000772 12709788 NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_provenance.
- NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_assertion wasDerivedFrom befree-20150227 NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_provenance.
- NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_assertion wasGeneratedBy ECO_0000203 NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP219013.RAoaxqUUb2ThZ5V2SPoE1TpGu2kba56MLyF4XHbJMJaT4130_provenance.