Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_provenance.
- NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_assertion description "[Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_provenance.
- NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_assertion evidence source_evidence_literature NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_provenance.
- NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_assertion SIO_000772 15009458 NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_provenance.
- NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_assertion wasDerivedFrom befree-2016 NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_provenance.
- NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_assertion wasGeneratedBy ECO_0000203 NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_provenance.
- befree-2016 importedOn "2016-02-19" NP434825.RAJBTt7FF7atb_iZHRWs3t7YW7QAEJXqU6mpquBe2NhsM130_provenance.