Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_provenance.
- NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_assertion wasGeneratedBy ECO_0000203 NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_provenance.
- NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_assertion wasDerivedFrom befree-20140225 NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_provenance.
- NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_assertion SIO_000772 12140678 NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_provenance.
- NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_assertion evidence source_evidence_literature NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_provenance.
- NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_assertion description "[The frequency of SCA8 expansion accounts for approximately 4.3 % of the whole pool of our ataxia families (2 out of 46), while none of the 127 controls screened carried > 35 CTG+CTA repeats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP323944.RAE0lVAESLr6rMotOjtRXGSguIWLkNQgPW_kMHB5DhqXc130_provenance.