Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance.
- NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance.
- NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_assertion evidence source_evidence_literature NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance.
- NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_assertion SIO_000772 20857310 NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance.
- NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_assertion wasDerivedFrom befree-2016 NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance.
- NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_assertion wasGeneratedBy ECO_0000203 NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance.
- befree-2016 importedOn "2016-02-19" NP840721.RA3J7PJTLiGSyLOCFfxIhQb0XpXBlKX1vjNkfNz8KCJgE130_provenance.