Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_provenance.
- NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_assertion description "[Our results suggest that a loss-of-function mutation in MASS1 might be responsible for the seizure phenotypes, though it is not likely that MASS1 contributed to the cause of febrile seizures in most of our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_provenance.
- NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_assertion evidence source_evidence_literature NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_provenance.
- NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_assertion SIO_000772 12402266 NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_provenance.
- NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_assertion wasDerivedFrom befree-2016 NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_provenance.
- NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_assertion wasGeneratedBy ECO_0000203 NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_provenance.
- befree-2016 importedOn "2016-02-19" NP372529.RAnqRBt_D4bDapzE74vWjFjpZAA7mdwNjBI_DtxD1PCsE130_provenance.