Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_provenance.
- NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_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." NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_provenance.
- NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_assertion evidence source_evidence_curated NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_provenance.
- NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_assertion SIO_000772 19158808 NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_provenance.
- NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_assertion wasDerivedFrom uniprot-20150221 NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_provenance.
- NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_assertion wasGeneratedBy ECO_0000218 NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP3427.RAnmODJ3q2vHqNYouP6Cd_gk0TxJWIQ9bab654mVb6Vic130_provenance.