Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_provenance.
- NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_assertion description "[The cytogenetic expression of the folate sensitive fragile site, FRAXE, is due to the expansion of a GCC repeat in proximal Xq28 of the human X chromosome and is associated with a mild form of mental handicap.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_provenance.
- NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_assertion evidence source_evidence_literature NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_provenance.
- NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_assertion SIO_000772 8824884 NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_provenance.
- NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_assertion wasDerivedFrom befree-20150227 NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_provenance.
- NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_assertion wasGeneratedBy ECO_0000203 NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412870.RAHtxU_d6wtfOwGJWpAEZbRwWGyP2Y3CAIyQ7btdGlwXM130_provenance.