Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion evidence source_evidence_literature NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion SIO_000772 19378506 NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion wasDerivedFrom befree-20140225 NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion wasGeneratedBy ECO_0000203 NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.