Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_assertion> ?p ?o ?g. }
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- NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_assertion type Assertion NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_head.
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- NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_assertion wasDerivedFrom gad-20150221 NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.
- NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_assertion SIO_000772 16596945 NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_provenance.
- NP99851.RAs5kXCDZrl0K9QShVinpT0TK9O20Swtj7Exdtiug9JyM130_assertion evidence source_evidence_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.