Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP800180.RAibqInW-OVY4B4A7UxJXABFqha89DaS564BYi6py-gmo130_assertion> ?p ?o ?g. }
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- NP800180.RAibqInW-OVY4B4A7UxJXABFqha89DaS564BYi6py-gmo130_assertion type Assertion NP800180.RAibqInW-OVY4B4A7UxJXABFqha89DaS564BYi6py-gmo130_head.
- NP800180.RAibqInW-OVY4B4A7UxJXABFqha89DaS564BYi6py-gmo130_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." NP800180.RAibqInW-OVY4B4A7UxJXABFqha89DaS564BYi6py-gmo130_provenance.
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- NP800180.RAibqInW-OVY4B4A7UxJXABFqha89DaS564BYi6py-gmo130_assertion SIO_000772 23312802 NP800180.RAibqInW-OVY4B4A7UxJXABFqha89DaS564BYi6py-gmo130_provenance.
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