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- source_evidence_literature type ECO_0000212 NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_provenance.
- NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_assertion description "[Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_provenance.
- NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_assertion evidence source_evidence_literature NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_provenance.
- NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_assertion SIO_000772 19196735 NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_provenance.
- NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_assertion wasDerivedFrom befree-20150227 NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_provenance.
- NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_assertion wasGeneratedBy ECO_0000203 NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_provenance.
- befree-20150227 importedOn "2015-02-27" NP948404.RACnwcaHbRHO-HKSqKP0p9acamgIQyAs3bQurMt5S6W38130_provenance.