Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_provenance.
- NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_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." NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_provenance.
- NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_assertion evidence source_evidence_literature NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_provenance.
- NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_assertion SIO_000772 19158808 NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_provenance.
- NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_assertion wasDerivedFrom befree-20150227 NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_provenance.
- NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_assertion wasGeneratedBy ECO_0000203 NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP371538.RAVPHDNKEKIDlFkydlYTVVvyjPcHb7yoe9nYQz2LBODhs130_provenance.