Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_provenance.
- NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_assertion description "[Dermatosparaxis is a recessively inherited connective-tissue disorder that results from lack of the activity of type I procollagen N-proteinase, the enzyme that removes the amino-terminal propeptides from type I procollagen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_provenance.
- NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_assertion evidence source_evidence_literature NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_provenance.
- NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_assertion SIO_000772 1642226 NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_provenance.
- NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_assertion wasDerivedFrom befree-2016 NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_provenance.
- NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_assertion wasGeneratedBy ECO_0000203 NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_provenance.
- befree-2016 importedOn "2016-02-19" NP531673.RAva0jNCBaC92zjhUVUv3TiNlenIwQQ3MSRQo8g-uJcss130_provenance.