Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_provenance.
- NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_assertion description "[LMNA mutations should be considered in the genetic screening of patients with familial DC without conduction system disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_provenance.
- NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_assertion evidence source_evidence_literature NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_provenance.
- NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_assertion SIO_000772 15219508 NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_provenance.
- NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_assertion wasDerivedFrom befree-2016 NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_provenance.
- NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_assertion wasGeneratedBy ECO_0000203 NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_provenance.
- befree-2016 importedOn "2016-02-19" NP449847.RASixaHslPpX_CuIczGN11xnco9MXrWRQmI8d3Kykrl2g130_provenance.