Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_provenance.
- NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_assertion description "[In one of the patients, the PRKAR1A gene responsible for Carney Complex and the KCNJ2 gene causal for Andersen syndrome are deleted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_provenance.
- NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_assertion evidence source_evidence_literature NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_provenance.
- NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_assertion SIO_000772 22166941 NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_provenance.
- NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_assertion wasDerivedFrom befree-2016 NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_provenance.
- NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_assertion wasGeneratedBy ECO_0000203 NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_provenance.
- befree-2016 importedOn "2016-02-19" NP946385.RACUlARUmhnuSyUWPtJVdeg1VCAnySSZ-wTY6939UwxB8130_provenance.