Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_assertion> ?p ?o ?g. }
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- NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_assertion type Assertion NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_head.
- NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_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." NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_provenance.
- NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_assertion evidence source_evidence_literature NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_provenance.
- NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_assertion SIO_000772 23312802 NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_provenance.
- NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_assertion wasDerivedFrom befree-20140225 NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_provenance.
- NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_assertion wasGeneratedBy ECO_0000203 NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_provenance.