@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o130_head
{
this:
np:hasAssertion
dgn-np:NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o130_assertion
a
np:Assertion
.
dgn-np:NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o130_provenance
a
np:Provenance
.
dgn-np:NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o130_assertion
{
miriam-gene:55054
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN74eca7288997153658215a8c651e38c2
sio:SIO_000628
miriam-gene:55054
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o130_provenance
{
dgn-np:NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o130_assertion
dcterms:description
"[The use of techniques such as whole genome association studies to perform broad, unbiased screening for the contributions of common genetic variations to complex disease has rapidly assisted in the identification of several novel susceptibility loci associated with pediatric-onset Crohn's disease such as IL23R and ATG16L1.]. 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:17600381
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP617714.RACnYiVV1S5mk8ZWn48sXToGulKf_BcDsMinsvEHda69o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:25+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}