@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM
> .
@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 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:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_head
{
this:
np:hasAssertion
dgn-np:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_assertion
;
np:hasProvenance
dgn-np:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance
;
np:hasPublicationInfo
dgn-np:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_assertion
a
np:Assertion
.
dgn-np:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance
a
np:Provenance
.
dgn-np:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_assertion
{
miriam-gene:355
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN3a772c6af7fdd6a320776667a81a6854
sio:SIO_000628
miriam-gene:355
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance
{
dgn-np:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_assertion
dct:description
"[We found no strong evidence of association for any of these loci with AD in this population. While the possibility exists that the genes analysed are involved in AD (ie they have weak effects and/or are population specific), results reinforce the need for extensive replication studies if we are to be successful in defining true risk factors in complex diseases.]. 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:11436125
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}