NP362937.RAUuIaWxgY-IeWCOsdODPOffm-YuhYsSpubOsiELpfcpQ
type: Nanopublication
has assertion: NP362937.RAUuIaWxgY-IeWCOsdODPOffm-YuhYsSpubOsiELpfcpQ130 assertion
has provenance: NP362937.RAUuIaWxgY-IeWCOsdODPOffm-YuhYsSpubOsiELpfcpQ130 provenance
has publication info: NP362937.RAUuIaWxgY-IeWCOsdODPOffm-YuhYsSpubOsiELpfcpQ130 publicationInfo
created: 2016-05-13T12:44:30+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetv3.0rdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v4.0.0.0

NP362937.RAUuIaWxgY-IeWCOsdODPOffm-YuhYsSpubOsiELpfcpQ130 assertion
type: Assertion
description: [CAA occurs in several familial conditions, including hereditary cerebral hemorrhage with amyloidosis of Icelandic type caused by deposition of mutant cystatin C, hereditary cerebral hemorrhage with amyloidosis Dutch type and familial AD with deposition of either A beta variants or wild-type A beta, the transthyretin-related meningo-vascular amyloidoses, gelsolin as well as familial prion disease-related CAAs and the recently described BRI2 gene-related CAAs in familial British dementia and familial Danish dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12146803
was generated by: ECO_0000203

befree-2016
imported on: 2016-02-19

DisGeNET evidence - LITERATURE
type: ECO_0000212
comment: Gene-disease associations inferred from text-mining the literature.

disgenetv3.0rdf
version: v4.0.0