@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8
> .
@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:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_head
{
this:
np:hasAssertion
dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_assertion
;
np:hasProvenance
dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_provenance
;
np:hasPublicationInfo
dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_assertion
a
np:Assertion
.
dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_provenance
a
np:Provenance
.
dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGN0dd17f67243613b2e8cb31c825d7bacf
sio:SIO_000628
miriam-gene:4846
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_provenance
{
dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_assertion
dcterms:description
"[In particular, the presence of eNOS TT894 genotype in patients with cognitive decline resulted significantly associated with increased plasma Hcy levels when compared with controls having the same genotype or patients having other eNOS genotypes (P = 0.02).]. 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:21607713
;
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:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:20+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" .
}