@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE
> .
@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:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_head
{
this:
np:hasAssertion
dgn-np:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_assertion
;
np:hasProvenance
dgn-np:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_provenance
;
np:hasPublicationInfo
dgn-np:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_assertion
a
np:Assertion
.
dgn-np:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_provenance
a
np:Provenance
.
dgn-np:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_assertion
{
miriam-gene:2195
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGN245fa1c7a46ce10e3aa1038c910a153c
sio:SIO_000628
miriam-gene:2195
,
lld:C0005586
;
a
sio:SIO_001122
.
}
dgn-np:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_provenance
{
dgn-np:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_assertion
dcterms:description
"[our results support an involvement of variation at the FAT gene in the etiology of BPAD, but that further work is needed both to clarify possible reasons for the observed risk allele differences and to ultimately identify the functionally relevant variant(s).]. 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:17938632
;
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:NP70645.RA172X8b5VTEuBx6jhFEEJAZ2bEVeRRclKnxHyvnm_kCE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:34+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" .
}