Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_provenance.
- NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_assertion description "[Our results demonstrate that SLS is caused by a strikingly heterogeneous group of mutations in the FALDH gene and provide a framework for understanding the genetic basis of SLS and the development of DNA-based diagnostic tests.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_provenance.
- NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_assertion evidence source_evidence_literature NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_provenance.
- NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_assertion SIO_000772 10577908 NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_provenance.
- NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_assertion wasDerivedFrom befree-2016 NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_provenance.
- NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_assertion wasGeneratedBy ECO_0000203 NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_provenance.
- befree-2016 importedOn "2016-02-19" NP268597.RACo-g9mP4thWTIHAQsHbP_zUtTPAUTBO5WHaK-DeVxvw130_provenance.