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- source_evidence_literature type ECO_0000212 NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_provenance.
- NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_assertion description "[These findings suggest that the FMR-1 mutation causing the fragile X syndrome leads to observable changes in neuroanatomy that may be relevant to the neurodevelopmental disability and behavioural problems observed in affected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_provenance.
- NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_assertion evidence source_evidence_literature NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_provenance.
- NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_assertion SIO_000772 7585014 NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_provenance.
- NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_assertion wasDerivedFrom befree-2016 NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_provenance.
- NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_assertion wasGeneratedBy ECO_0000203 NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_provenance.
- befree-2016 importedOn "2016-02-19" NP1313707.RAACBgSHkoKIXfWOeQZ6U_JZ-b_Xvt6cEURUPXmJNts9M130_provenance.