Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_provenance.
- NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_assertion description "[Mantle cell lymphoma with t(11;14) and unmutated or mutated VH genes expresses AID and undergoes isotype switch events.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_provenance.
- NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_assertion evidence source_evidence_literature NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_provenance.
- NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_assertion SIO_000772 14551145 NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_provenance.
- NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_assertion wasDerivedFrom befree-2016 NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_provenance.
- NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_assertion wasGeneratedBy ECO_0000203 NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_provenance.
- befree-2016 importedOn "2016-02-19" NP416376.RA4wGBvheCQq2J63jhhmMHVmOlN9tUNalun7FjbRwrY0I130_provenance.