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- source_evidence_literature type ECO_0000212 NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_provenance.
- NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involve]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_provenance.
- NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_assertion evidence source_evidence_literature NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_provenance.
- NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_assertion SIO_000772 17903297 NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_provenance.
- NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_assertion wasDerivedFrom gad-20150221 NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_provenance.
- NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_assertion wasGeneratedBy ECO_0000203 NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP156697.RAUs1AQL-u_IgJEDu02Euw-WAEcKtwictp_DiuH19sPn8130_provenance.