Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance.
- NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_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." NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance.
- NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_assertion evidence source_evidence_literature NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance.
- NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_assertion SIO_000772 19378506 NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance.
- NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_assertion wasDerivedFrom befree-2016 NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance.
- NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_assertion wasGeneratedBy ECO_0000203 NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance.
- befree-2016 importedOn "2016-02-19" NP733327.RAGm3togck7zAS4MIl1BC6iYz0KDlEdSl7oGtcUpsKXRw130_provenance.