Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance.
- NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance.
- NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_assertion evidence source_evidence_literature NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance.
- NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_assertion SIO_000772 10480368 NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance.
- NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_assertion wasDerivedFrom befree-20140225 NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance.
- NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_assertion wasGeneratedBy ECO_0000203 NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance.