Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_assertion> ?p ?o ?g. }
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- NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_assertion type Assertion NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_head.
- 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.