Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_provenance.
- NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_assertion description "[Our results suggest that mutations in FMR-1 are directly responsible for fragile X syndrome, irrespective of possible secondary effects caused by FRAXA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_provenance.
- NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_assertion evidence source_evidence_literature NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_provenance.
- NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_assertion SIO_000772 8490650 NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_provenance.
- NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_assertion wasDerivedFrom befree-2016 NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_provenance.
- NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_assertion wasGeneratedBy ECO_0000203 NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_provenance.
- befree-2016 importedOn "2016-02-19" NP1343148.RACES6xp3y8iR50bvSTW6RjX522FbhQkU6mFaPfcZsLME130_provenance.