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- source_evidence_literature type ECO_0000212 NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_provenance.
- NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_assertion description "[Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_provenance.
- NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_assertion evidence source_evidence_literature NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_provenance.
- NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_assertion SIO_000772 19158808 NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_provenance.
- NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_assertion wasDerivedFrom befree-2016 NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_provenance.
- NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_assertion wasGeneratedBy ECO_0000203 NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_provenance.
- befree-2016 importedOn "2016-02-19" NP715791.RA3r9c1PIUMl9RPprBiHtx-HjrpO3cBeuJ0Jw3Q56F7oU130_provenance.