Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion wasGeneratedBy ECO_0000203 NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion wasDerivedFrom befree-20150227 NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion SIO_000772 10399872 NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion evidence source_evidence_literature NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.