Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_provenance.
- NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_assertion description "[Hereditary spastic paraplegia (HSP) with thin corpus callosum (TCC) and mental impairment is a frequent subtype of complicated HSP, often inherited as an autosomal recessive (AR) trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_provenance.
- NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_assertion evidence source_evidence_literature NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_provenance.
- NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_assertion SIO_000772 20593214 NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_provenance.
- NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_assertion wasDerivedFrom befree-20140225 NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_provenance.
- NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_assertion wasGeneratedBy ECO_0000203 NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP542332.RAU5Sh9Bnn1dC5men60UJr9xxOqh0zEelLbEFOUdxDbH4130_provenance.