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- source_evidence_literature type ECO_0000212 NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_provenance.
- NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_assertion description "[Biofluid studies identify about 15% of patients with FTLD due to a genetic mutation that is associated with the specific histopathologic features of TDP-43 or a tauopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_provenance.
- NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_assertion evidence source_evidence_literature NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_provenance.
- NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_assertion SIO_000772 21833654 NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_provenance.
- NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_assertion wasDerivedFrom befree-2016 NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_provenance.
- NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_assertion wasGeneratedBy ECO_0000203 NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_provenance.
- befree-2016 importedOn "2016-02-19" NP916343.RAeDzNzheeSq9Jt_w0ORdOEvOkKl6hu1d3Sen04sJUlNI130_provenance.