Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_provenance.
- NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_assertion description "[Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_provenance.
- NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_assertion evidence source_evidence_literature NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_provenance.
- NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_assertion SIO_000772 15850581 NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_provenance.
- NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_assertion wasDerivedFrom befree-20150227 NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_provenance.
- NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_assertion wasGeneratedBy ECO_0000203 NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP647714.RAb9x5atGFgcz9DVPRFZ0tqC58xUGvq6IqmT3sPxJ_nbs130_provenance.