Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_provenance.
- NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_assertion description "[Peripheral neuropathy in hereditary spastic paraplegia due to spastin (SPG4) mutation--a neurophysiological study using excitability techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_provenance.
- NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_assertion evidence source_evidence_literature NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_provenance.
- NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_assertion SIO_000772 22192498 NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_provenance.
- NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_assertion wasDerivedFrom befree-20150227 NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_provenance.
- NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_assertion wasGeneratedBy ECO_0000203 NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710002.RAQcWLjo2sbO5r3WIno-p-0yMpj8v3Sr117VFVh1XHSvg130_provenance.