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- source_evidence_literature type ECO_0000212 NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_provenance.
- NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_assertion description "[Also, AD and PD clinical diagnoses in patients who carry PGRN null mutations likely result from etiologic heterogeneity rather than PGRN haploinsufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_provenance.
- NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_assertion evidence source_evidence_literature NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_provenance.
- NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_assertion SIO_000772 17923627 NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_provenance.
- NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_assertion wasDerivedFrom befree-20140225 NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_provenance.
- NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_assertion wasGeneratedBy ECO_0000203 NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_provenance.