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- source_evidence_literature type ECO_0000212 NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_provenance.
- NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_assertion description "[Despite the difference in phenotypes, there remains a possibility that the causative gene for these Japanese SCA is allelic to SCA15.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_provenance.
- NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_assertion evidence source_evidence_literature NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_provenance.
- NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_assertion SIO_000772 14981189 NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_provenance.
- NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_assertion wasDerivedFrom befree-20140225 NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_provenance.
- NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_assertion wasGeneratedBy ECO_0000203 NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP937519.RAxP7tThfEG625CcMLVR_tutIdpt9nu7zi56m_R_-LXf0130_provenance.