Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_provenance.
- NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_assertion description "[Three individuals (2.6%) with the FRAXA form of the fragile X syndrome and one boy (0.9%) with FRAXE mental retardation were detected; a total of four newly diagnosed fragile X families were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_provenance.
- NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_assertion evidence source_evidence_literature NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_provenance.
- NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_assertion SIO_000772 12113322 NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_provenance.
- NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_assertion wasDerivedFrom befree-20150227 NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_provenance.
- NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_assertion wasGeneratedBy ECO_0000203 NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_provenance.
- befree-20150227 importedOn "2015-02-27" NP409174.RASmK10mMo4e5xNHJJWJ23vI1dG1UKRu107WY6rY9Bp28130_provenance.