Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_provenance.
- NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_assertion description "[At present, eight different genes causing ADCAs have been found: spinocerebeller ataxia type 1 (SCA1), SCA2, SCA3/Machado-Joseph disease (MJD), SCA6, SCA7, SCA8, SCA12 and dentatorubropallidoluysian atrophy (DRPLA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_provenance.
- NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_assertion evidence source_evidence_literature NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_provenance.
- NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_assertion SIO_000772 11018707 NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_provenance.
- NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_assertion wasDerivedFrom befree-20150227 NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_provenance.
- NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_assertion wasGeneratedBy ECO_0000203 NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681813.RArkNkJQ7h3NQiOONI6VljNd3imMFC8bd_Yp3Np_g_esU130_provenance.