Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_provenance.
- NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_assertion wasGeneratedBy ECO_0000203 NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_provenance.
- NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_assertion wasDerivedFrom befree-20140225 NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_provenance.
- NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_assertion SIO_000772 20660572 NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_provenance.
- NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_assertion evidence source_evidence_literature NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_provenance.
- NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_assertion description "[In the NET-Registry, 9/101 patients (8.9%) with ICTs had germline mutations, 8 in MEN1 and 1 in VHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP819977.RAX1xHI34-S0IDDrdPM8wPRzGii4x-d1g3Yxzj_OoGnvM130_provenance.