Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_provenance.
- NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_assertion description "[Our findings expand the number of large FBN1 deletions, and emphasize the importance of screening for large genomic deletions in connective tissue disorders featuring aortopathies, especially for those with classic Marfan phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_provenance.
- NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_assertion evidence source_evidence_literature NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_provenance.
- NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_assertion SIO_000772 21936929 NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_provenance.
- NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_assertion wasDerivedFrom befree-20150227 NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_provenance.
- NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_assertion wasGeneratedBy ECO_0000203 NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP395748.RAfndqWXupjSSyqTUmCdyEv5KGeAxuuzVeqQDUiMuNQQY130_provenance.