Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_provenance.
- NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_assertion description "[The expansion of a CAG repeat upstream of the PP2APR55beta gene has been recently reported as a novel cause of a dominantly inherited ataxia (SCA12) in a kindred with limb tremor as an early feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_provenance.
- NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_assertion evidence source_evidence_literature NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_provenance.
- NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_assertion SIO_000772 11708992 NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_provenance.
- NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_assertion wasDerivedFrom befree-20140225 NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_provenance.
- NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_assertion wasGeneratedBy ECO_0000203 NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP910439.RAti_kwqrN4FCor31xfixEAuIT7hTpS1WB-vT0j_T1xIk130_provenance.