Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_provenance.
- NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_assertion description "[These data suggest including detection of p130/131 as a criterion for the diagnosis of probable CJD in addition to the currently accepted criteria of a rapidly progressive dementia of less than 2 years duration, typical neurological signs, and periodic sharp-wave complexes in the EEG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_provenance.
- NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_assertion evidence source_evidence_literature NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_provenance.
- NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_assertion SIO_000772 8826809 NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_provenance.
- NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_assertion wasDerivedFrom befree-20140225 NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_provenance.
- NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_assertion wasGeneratedBy ECO_0000203 NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_provenance.
- befree-20140225 importedOn "2014-02-25" NP269233.RAZznXQa_LdWdcwWqRNUS8ydKc-NKn1HDqdC_IgOP9e04130_provenance.