Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_provenance.
- NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_assertion description "[This region contains the genes of FAM84A, NBAS, DDX1, MYCNOS and MYCN, of which haploinsufficiency or mutations of the MYCN gene is associated with Feingold syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_provenance.
- NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_assertion evidence source_evidence_literature NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_provenance.
- NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_assertion SIO_000772 22842076 NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_provenance.
- NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_assertion wasDerivedFrom befree-20150227 NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_provenance.
- NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_assertion wasGeneratedBy ECO_0000203 NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP582733.RA1HmZKvHKupV3jac1VNhUOorE7SZ6WB-BIKDAP-DdTWQ130_provenance.