Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_provenance.
- NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_assertion description "[Screening for functional sequence variations and mutations in ABCA1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_provenance.
- NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_assertion evidence source_evidence_literature NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_provenance.
- NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_assertion SIO_000772 15262183 NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_provenance.
- NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_assertion wasDerivedFrom gad-20130706 NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_provenance.
- NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_assertion wasGeneratedBy ECO_0000203 NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP89697.RAQtevPmddDNJcks7SLBMs0DwpZeQBTGz-0XCh3pXzcQk130_provenance.