@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc
> .
@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:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_head
{
this:
np:hasAssertion
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_assertion
;
np:hasProvenance
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_provenance
;
np:hasPublicationInfo
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_assertion
a
np:Assertion
.
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_provenance
a
np:Provenance
.
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_assertion
{
miriam-gene:79068
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGNb3d1ba6447de1a29c3c6fe69db3151d1
sio:SIO_000628
miriam-gene:79068
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_provenance
{
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_assertion
dcterms:description
"[In a sample of 8,364 white and 2,083 African American men and women with no clinical history of stroke, significantly greater mean change in performance on the Delayed Word Recall Test was associated with 2 of 4 FTO single nucleotide polymorphisms examined (rs9939609, rs805136, rs17817449, and rs1421085) in whites but not in African Americans (p ≤ 0.002).]. 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:23136261
;
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:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:07+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" .
}