Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance.
- NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance.
- NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_assertion evidence source_evidence_literature NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance.
- NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_assertion SIO_000772 18714162 NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance.
- NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_assertion wasDerivedFrom befree-2016 NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance.
- NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_assertion wasGeneratedBy ECO_0000203 NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance.
- befree-2016 importedOn "2016-02-19" NP688598.RAMbgWJC_br8shPH4_qa0IuiwDxkUmGMRJDzOsXraLMyc130_provenance.