Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_provenance.
- NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_assertion description "[The most common cause of inherited SCA was a mutation at the SCA6 locus (25%), followed by mutation at the SCA1 locus (15%), SCA3 locus (5%) and dentatorubral-pallidoluysian atrophy locus (5%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_provenance.
- NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_assertion evidence source_evidence_literature NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_provenance.
- NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_assertion SIO_000772 11359084 NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_provenance.
- NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_assertion wasDerivedFrom befree-20140225 NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_provenance.
- NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_assertion wasGeneratedBy ECO_0000203 NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_provenance.
- befree-20140225 importedOn "2014-02-25" NP389167.RAHfaMI5nOnsW7A9pmrvpnumlPCy8PT1oQiYY4diklWos130_provenance.