Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_provenance.
- NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_assertion description "[Spinal muscular atrophy (SMA) is a common inherited neuromuscular disorder caused by homozygous loss of function of the survival motor neuron 1 (SMN1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_provenance.
- NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_assertion evidence source_evidence_literature NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_provenance.
- NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_assertion SIO_000772 17924536 NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_provenance.
- NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_assertion wasDerivedFrom befree-2016 NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_provenance.
- NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_assertion wasGeneratedBy ECO_0000203 NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_provenance.
- befree-2016 importedOn "2016-02-19" NP634479.RA1qDBUSwwS55yiK3XmOtSON7YSLW2zl6IeLiStN2reIM130_provenance.