Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_provenance.
- NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_assertion description "[Our data add new variants to the repertoire of ADAR mutations in DSH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_provenance.
- NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_assertion evidence source_evidence_literature NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_provenance.
- NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_assertion SIO_000772 15146470 NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_provenance.
- NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_assertion wasDerivedFrom befree-20140225 NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_provenance.
- NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_assertion wasGeneratedBy ECO_0000203 NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_provenance.
- befree-20140225 importedOn "2014-02-25" NP260262.RA0VbKH-BMoZ1DrDlI5V--omVhoDLt4zAzHLZRZVDiC58130_provenance.