Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_provenance.
- NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_assertion description "[Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_provenance.
- NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_assertion evidence source_evidence_literature NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_provenance.
- NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_assertion SIO_000772 23603762 NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_provenance.
- NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_assertion wasDerivedFrom befree-20140225 NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_provenance.
- NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_assertion wasGeneratedBy ECO_0000203 NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP398997.RAyGLZbQ6OeJE9z_kXGifqFslypyx__PQHqRDHbcswsTg130_provenance.