Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_provenance.
- NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_assertion description "[The disease is characterized by selective loss of spinal cord motor neurons leading to muscle atrophy and is the result of mutations in the survival motor neuron (SMN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_provenance.
- NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_assertion evidence source_evidence_literature NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_provenance.
- NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_assertion SIO_000772 16108074 NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_provenance.
- NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_assertion wasDerivedFrom befree-20150227 NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_provenance.
- NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_assertion wasGeneratedBy ECO_0000203 NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP531735.RAMg5Ib33H8ZOiu-2U5OlIKkO6pGM7OWtM8QrylslS9gM130_provenance.