Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_provenance.
- NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_assertion description "[Given the complexity of HDGC, not only with regard to the management of the DGC risk, but also with regard to the risk for other related cancers, such as LBC, a multi-disciplinary approach is needed for the management of individuals with known CDH1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_provenance.
- NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_assertion evidence source_evidence_literature NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_provenance.
- NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_assertion SIO_000772 18046629 NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_provenance.
- NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_assertion wasDerivedFrom befree-2016 NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_provenance.
- NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_assertion wasGeneratedBy ECO_0000203 NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_provenance.
- befree-2016 importedOn "2016-02-19" NP642613.RAsD_2h5IcW_ua55wqBsD7AlMt6uzcDUXu6BjMdFdKeiw130_provenance.