Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_provenance.
- NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_assertion description "[Further study of the pathological mechanisms of the mutant forms of seipin may lead to important new insights into motor neuron diseases, including other spastic paraplegia diseases and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_provenance.
- NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_assertion evidence source_evidence_literature NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_provenance.
- NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_assertion SIO_000772 18790819 NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_provenance.
- NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_assertion wasDerivedFrom befree-2016 NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_provenance.
- NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_assertion wasGeneratedBy ECO_0000203 NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_provenance.
- befree-2016 importedOn "2016-02-19" NP692960.RAPScCuCOxjWtmmtQnvFBVJSzW7-YLM4MAlVHG59_Y4DU130_provenance.