Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_provenance.
- NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_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." NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_provenance.
- NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_assertion evidence source_evidence_literature NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_provenance.
- NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_assertion SIO_000772 8824884 NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_provenance.
- NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_assertion wasDerivedFrom befree-20150227 NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_provenance.
- NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_assertion wasGeneratedBy ECO_0000203 NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP409260.RAV8I7dcfRctmS5bmEuga989UhA6iivBJa94MBIDSrRbA130_provenance.