Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_provenance.
- NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_assertion description "[Autosomal recessive spastic paraplegias (ARHSPs) usually have clinically complex phenotypes but the SPG5, SPG24, and SPG28 loci are considered to be associated with pure forms of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_provenance.
- NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_assertion evidence source_evidence_literature NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_provenance.
- NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_assertion SIO_000772 17503452 NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_provenance.
- NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_assertion wasDerivedFrom befree-20140225 NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_provenance.
- NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_assertion wasGeneratedBy ECO_0000203 NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP182774.RAHl8tUqcElG_BtkYGDwKk0bwJIwGl-_nW2fkWMY60-gk130_provenance.