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- source_evidence_literature type ECO_0000212 NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_provenance.
- NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_assertion description "[Alu-specific microhomology-mediated deletion of the final exon of SPAST in three unrelated subjects with hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_provenance.
- NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_assertion evidence source_evidence_literature NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_provenance.
- NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_assertion SIO_000772 21659953 NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_provenance.
- NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_assertion wasDerivedFrom befree-2016 NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_provenance.
- NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_assertion wasGeneratedBy ECO_0000203 NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_provenance.
- befree-2016 importedOn "2016-02-19" NP900869.RAlAzuUO-QGr5jrA1jdCz9DdgrhHl0Hbwj9VnKIhQ5Eys130_provenance.