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- source_evidence_literature type ECO_0000212 NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_provenance.
- NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_assertion description "[From the clinical point of view, the folate sensitive rare fragile site FRAXA is the most important fragile site as it is associated with the fragile X syndrome, the most common form of familial mental retardation, affecting about 1/4000 males and 1/6000 females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_provenance.
- NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_assertion evidence source_evidence_literature NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_provenance.
- NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_assertion SIO_000772 18078840 NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_provenance.
- NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_assertion wasDerivedFrom befree-20140225 NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_provenance.
- NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_assertion wasGeneratedBy ECO_0000203 NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP171610.RA_Tyol_39D7robOiJgamh1CugIPXuI7tliUmKtUNodkg130_provenance.