Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion description "[They include well-recognized syndromes such as tuberous sclerosis complex, epilepsy associated with Rett syndrome, some of the progressive myoclonic epilepsies, and novel disorders such as epilepsy associated with mutations in the PCDH 19 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion evidence source_evidence_literature NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion SIO_000772 22946725 NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion wasDerivedFrom befree-20140225 NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion wasGeneratedBy ECO_0000203 NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.