Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_assertion> ?p ?o ?g. }
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- NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_assertion type Assertion NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_head.
- NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_provenance.
- NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_assertion evidence source_evidence_literature NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_provenance.
- NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_assertion SIO_000772 23312802 NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_provenance.
- NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_assertion wasDerivedFrom befree-2016 NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_provenance.
- NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_assertion wasGeneratedBy ECO_0000203 NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_provenance.