@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk
> .
@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:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_head
{
this:
np:hasAssertion
dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_assertion
;
np:hasProvenance
dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_provenance
;
np:hasPublicationInfo
dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_assertion
a
np:Assertion
.
dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_provenance
a
np:Provenance
.
dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_assertion
{
miriam-gene:7099
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGN162d133423ed223047b933328de3e9ea
sio:SIO_000628
miriam-gene:7099
,
lld:C0009324
;
a
sio:SIO_001122
.
}
dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_provenance
{
dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_assertion
dcterms:description
"[We observed that the R702W and 1007fs Nod2 alleles and the A299G Tlr4 alleles were significantly more prevalent in patients with CD as compared to healthy controls or patients with ulcerative colitis.]. 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:16010583
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:30+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: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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}