Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_provenance.
- NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_assertion description "[In addition, they might reflect that other phenotypic features associated with CDKL5 mutations (Rett-like features, infantile spasm) or ARX mutations (dystonia, spasticity) are more distinctive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_provenance.
- NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_assertion evidence source_evidence_literature NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_provenance.
- NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_assertion SIO_000772 19734009 NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_provenance.
- NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_assertion wasDerivedFrom befree-20150227 NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_provenance.
- NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_assertion wasGeneratedBy ECO_0000203 NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835467.RAISi2ojOeb9Gh8FH7jDhtOaSpfi1iGwLIDArbZjE2nZI130_provenance.