NP164107.RAP33Dm6HxMk 1T1-CtUFqtn 6Tclr 3DAEVPVLwRS2-s
type: Nanopublication
has assertion: NP164107.RAP33Dm6HxMk 1T1-CtUFqtn 6Tclr 3DAEVPVLwRS2-s130 assertion
has provenance: NP164107.RAP33Dm6HxMk 1T1-CtUFqtn 6Tclr 3DAEVPVLwRS2-s130 provenance
has publication info: NP164107.RAP33Dm6HxMk 1T1-CtUFqtn 6Tclr 3DAEVPVLwRS2-s130 publicationInfo
created: 2016-05-13T12:43:01+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

NP164107.RAP33Dm6HxMk 1T1-CtUFqtn 6Tclr 3DAEVPVLwRS2-s130 assertion
type: Assertion
description: [Thrombophilia was identified in more than one-quarter (26.6% = 107/402) of the RPL subjects. APC-R not caused by FVL mutation was the most common thrombophilia marker in Malaysians, whereas in Caucasians it was the APC-R due to FVL mutation. The identific]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20144172
was generated by: ECO_0000203

gad-20150221
imported on: 2015-02-21

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

disgenetv3.0rdf
version: v4.0.0