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- source_evidence_literature type ECO_0000212 NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_provenance.
- NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_assertion wasGeneratedBy ECO_0000203 NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_provenance.
- NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_assertion wasDerivedFrom befree-20140225 NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_provenance.
- NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_assertion SIO_000772 24076603 NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_provenance.
- NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_assertion evidence source_evidence_literature NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_provenance.
- NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_assertion description "[Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP726793.RAQmHYi2PNgGSVo9lf-fSfO96xyjItKVi470aCnvbEmEc130_provenance.