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- source_evidence_literature type ECO_0000212 NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_provenance.
- NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_assertion description "[A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_provenance.
- NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_assertion evidence source_evidence_literature NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_provenance.
- NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_assertion SIO_000772 18200586 NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_provenance.
- NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_assertion wasDerivedFrom befree-2016 NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_provenance.
- NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_assertion wasGeneratedBy ECO_0000203 NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_provenance.
- befree-2016 importedOn "2016-02-19" NP650391.RAgFEs1e3cuwy3y35W_xL6nPnp3pyb476WZ4ma53aOy5U130_provenance.