Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_provenance.
- NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_assertion description "[Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_provenance.
- NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_assertion evidence source_evidence_literature NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_provenance.
- NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_assertion SIO_000772 15667412 NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_provenance.
- NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_assertion wasDerivedFrom befree-20140225 NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_provenance.
- NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_assertion wasGeneratedBy ECO_0000203 NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP368307.RAYmfmjJBx4m9f66azmwzY0511Rs0UL6AyYqTbPyFwXyQ130_provenance.