Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_provenance.
- NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_assertion description "[Dystrophin analysis in duchenne muscular dystrophy: use in fetal diagnosis and in genetic counseling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_provenance.
- NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_assertion evidence source_evidence_literature NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_provenance.
- NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_assertion SIO_000772 2672800 NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_provenance.
- NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_assertion wasDerivedFrom befree-2016 NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_provenance.
- NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_assertion wasGeneratedBy ECO_0000203 NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295861.RAQCu6-ReO8wJvXayZ9OR4R-xy_PXOQYFwYyI5DT4T_Sc130_provenance.