@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE
> .
@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:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_head
{
this:
np:hasAssertion
dgn-np:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_assertion
;
np:hasProvenance
dgn-np:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_provenance
;
np:hasPublicationInfo
dgn-np:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_assertion
a
np:Assertion
.
dgn-np:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_provenance
a
np:Provenance
.
dgn-np:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_assertion
{
miriam-gene:808
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN866e80909441b7b1ac8cf1b94dd2c9ff
sio:SIO_000628
miriam-gene:808
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_provenance
{
dgn-np:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_assertion
dcterms:description
"[Our findings provided further evidence on the association between CAM pathway and AD susceptibility, which would be helpful to study the genetic mechanisms of AD and may significantly assist in the development of therapeutic strategies.]. 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:22017384
;
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:NP449027.RAwyaULUBjHjut-JQY1TKWNfPfnbtu2AxTws9vRvC43IE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}