@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_head
{
this:
np:hasAssertion
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_assertion
;
np:hasProvenance
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_provenance
;
np:hasPublicationInfo
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_assertion
a
np:Assertion
.
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_provenance
a
np:Provenance
.
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_assertion
{
miriam-gene:2837
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN431eacce9f3c5c4cd2caf86620b641cb
sio:SIO_000628
miriam-gene:2837
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_provenance
{
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_assertion
dcterms:description
"[To assess the physiological relevance of an allelic variation in the KNS2 gene, the association analysis of three single nucleotide polymorphisms (SNPs) in the 5'UTR or in intronic sequences of KNS2 gene were performed in 100 AD brain patients and in 103 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:15364413
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP279106.RAfRVJJWUils2fEVoC3A4X0Mr4I8QiqHvar7Qw2OVN7wI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}