Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance.
- NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_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." NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance.
- NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_assertion evidence source_evidence_literature NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance.
- NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_assertion SIO_000772 19378506 NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance.
- NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_assertion wasDerivedFrom befree-20140225 NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance.
- NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_assertion wasGeneratedBy ECO_0000203 NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP603878.RAqK_I9bh1fXSle_HMVhfTVD8L2EdYS6xPFEgu2Zhwwcg130_provenance.