Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_provenance.
- NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_assertion description "[ATM mutations are rare in familial chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_provenance.
- NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_assertion evidence source_evidence_literature NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_provenance.
- NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_assertion SIO_000772 12091354 NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_provenance.
- NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_assertion wasDerivedFrom lhgdn-20090331 NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_provenance.
- NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_assertion wasGeneratedBy ECO_0000203 NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP195098.RAcV0uOpgCsHZSerAca3h8JLeGDTc-yxdEO0D2lj0vSUQ130_provenance.