Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_provenance.
- NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_assertion description "[Malignant mutation in the lamin A/C gene causing progressive conduction system disease and early sudden death in a family with mild form of limb-girdle muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_provenance.
- NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_assertion evidence source_evidence_literature NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_provenance.
- NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_assertion SIO_000772 17605093 NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_provenance.
- NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_assertion wasDerivedFrom befree-20150227 NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_provenance.
- NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_assertion wasGeneratedBy ECO_0000203 NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537766.RA2Kem0o3espFqd1LR7qW0VmI0m9m05QdO0QhEUkWggGE130_provenance.