Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_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." NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion evidence source_evidence_literature NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion SIO_000772 14576201 NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion wasDerivedFrom befree-2016 NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion wasGeneratedBy ECO_0000203 NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- befree-2016 importedOn "2016-02-19" NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.