@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4
> .
@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:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_head
{
this:
np:hasAssertion
dgn-np:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_assertion
;
np:hasProvenance
dgn-np:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_provenance
;
np:hasPublicationInfo
dgn-np:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_assertion
a
np:Assertion
.
dgn-np:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_provenance
a
np:Provenance
.
dgn-np:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_assertion
{
miriam-gene:27190
a
ncit:C16612
.
lld:C0007570
a
ncit:C7057
.
dgn-gda:DGN4fefd3fcad57802b96c95e269bbdba0d
sio:SIO_000628
miriam-gene:27190
,
lld:C0007570
;
a
sio:SIO_001122
.
}
dgn-np:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_provenance
{
dgn-np:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_assertion
dcterms:description
"[There were no statistically significant allele or haplotype frequency differences between cases and controls. Therefore, these results provide no evidence that these loci are associated with CD in this sample population.]. 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:15713213
;
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:NP63393.RA4JtCKwlzYNyBZvxWRCLC2SHjK-CUo_2F50IgxnlB6L4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}