Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion evidence source_evidence_literature NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion SIO_000772 17646629 NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion wasDerivedFrom befree-20140225 NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion wasGeneratedBy ECO_0000203 NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.