Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_provenance.
- NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_assertion description "[A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_provenance.
- NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_assertion evidence source_evidence_literature NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_provenance.
- NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_assertion SIO_000772 20593214 NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_provenance.
- NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_assertion wasDerivedFrom befree-20150227 NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_provenance.
- NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_assertion wasGeneratedBy ECO_0000203 NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP932988.RAapOJExKjAMh4Svt8Afbf5y5fv_-yVOUi2xATD0nqGvI130_provenance.