Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion description "[Mutations in the SPG7 gene, which encodes paraplegin, are responsible for an autosomal recessive hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion evidence source_evidence_literature NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion SIO_000772 16534102 NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion wasDerivedFrom befree-2016 NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion wasGeneratedBy ECO_0000203 NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- befree-2016 importedOn "2016-02-19" NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.