Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_assertion type Assertion NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_head.
- NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_assertion description "[These latter proteins include the ABri and ADan subunits in familial British dementia and familial Danish dementia, respectively, which are also known under the umbrella term BRI2 gene-related dementias, variant cystatin C in hereditary cerebral haemorrhage with amyloidosis of Icelandic-type, variant transthyretins in meningo-vascular amyloidosis, disease-associated prion protein (PrP(Sc)) in hereditary prion disease with premature stop codon mutations and mutated gelsolin (AGel) in familial amyloidosis of Finnish type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_provenance.
- NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_assertion evidence source_evidence_literature NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_provenance.
- NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_assertion SIO_000772 19225789 NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_provenance.
- NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_assertion wasDerivedFrom befree-20150227 NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_provenance.
- NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_assertion wasGeneratedBy ECO_0000203 NP647787.RA2mojJgWCAMl6WwIQp3h-LpU2XKz0e5k4IP3pbeEoEk0130_provenance.