Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_provenance.
- NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_assertion description "[Hereditary spastic paraplegia (HSP) with thin corpus callosum (HSP-TCC) is a frequent subtype of complicated HSP clinically characterised by slowly progressive spastic paraparesis with cognitive impairment and thin corpus callosum (TCC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_provenance.
- NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_assertion evidence source_evidence_literature NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_provenance.
- NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_assertion SIO_000772 19196735 NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_provenance.
- NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_assertion wasDerivedFrom befree-20140225 NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_provenance.
- NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_assertion wasGeneratedBy ECO_0000203 NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP937488.RA_wTPSLx2na_wfPlD-rwXVDdrK1E5v4rMabQmsDfMm0M130_provenance.