Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_provenance.
- NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_assertion description "[Among the 15 sporadic SCA patients, genetic mutations for SCA2, SCA6, SCA17, and SCA31 were identified, indicating that ADCAs should be considered in sporadic cases of ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_provenance.
- NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_assertion evidence source_evidence_literature NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_provenance.
- NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_assertion SIO_000772 21088341 NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_provenance.
- NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_assertion wasDerivedFrom befree-20150227 NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_provenance.
- NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_assertion wasGeneratedBy ECO_0000203 NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP739531.RA5RjSIydBBUijUVXFt12Tt0Eg0zcJoh6Zu--JnSWoIT8130_provenance.