Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_provenance.
- NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_assertion description "[Identification of mutations in DNA polymerase beta mRNAs from patients with Werner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_provenance.
- NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_assertion evidence source_evidence_literature NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_provenance.
- NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_assertion SIO_000772 7545922 NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_provenance.
- NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_assertion wasDerivedFrom befree-20140225 NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_provenance.
- NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_assertion wasGeneratedBy ECO_0000203 NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP596441.RA8DK8sGRzjCNK8ktgNCw-NEvxWkbhffCA4ccyqnPE1GU130_provenance.