@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8
> .
@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:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_head
{
this:
np:hasAssertion
dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_assertion
;
np:hasProvenance
dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_provenance
;
np:hasPublicationInfo
dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_assertion
a
np:Assertion
.
dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_provenance
a
np:Provenance
.
dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_assertion
{
miriam-gene:345651
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN0098e950323713b6e1d5ebbe4153333b
sio:SIO_000628
miriam-gene:345651
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_provenance
{
dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_assertion
dcterms:description
"[Given that a linkage signal for AAO has been detected near ACT, we hypothesized that ACT genetic variation affects AAO rather than disease risk and this may explain the previous inconsistent findings between ACT genetic variation and AD risk.]. 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:16137793
;
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:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}