Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.
- NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_assertion description "[Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.
- NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_assertion evidence source_evidence_literature NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.
- NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_assertion SIO_000772 16596945 NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.
- NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_assertion wasDerivedFrom gad-20150221 NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.
- NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_assertion wasGeneratedBy ECO_0000203 NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.