Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_assertion> ?p ?o ?g. }
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- NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_assertion type Assertion NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_head.
- NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_assertion description "[Functionally significant, rare transcription factor variants in tetralogy of Fallot.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_provenance.
- NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_assertion evidence source_evidence_curated NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_provenance.
- NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_assertion SIO_000772 25093829 NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_provenance.
- NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_assertion wasDerivedFrom ctd_human-20150221 NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_provenance.
- NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_assertion wasGeneratedBy ECO_0000218 NP15091.RA75pQEVEdRqb1ridofuaCIIvnFx6YXoHat17XqA9mt8g130_provenance.