@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA
> .
@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:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_head
{
this:
np:hasAssertion
dgn-np:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_assertion
;
np:hasProvenance
dgn-np:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_provenance
;
np:hasPublicationInfo
dgn-np:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_assertion
a
np:Assertion
.
dgn-np:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_provenance
a
np:Provenance
.
dgn-np:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_assertion
{
miriam-gene:915
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN5546f678b1893e0e38c3e214f39131f0
sio:SIO_000628
miriam-gene:915
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_provenance
{
dgn-np:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_assertion
dcterms:description
"[qRT-PCR conducted on all the samples confirmed that increased CD3D expression in affected samples was associated with NOD2(R) status, and that increased MUC1, DUOX2, DMBT1 and decreased C4orf7 expression in unaffected samples was associated with CD, independent of NOD2 status.]. 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:20155851
;
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:NP811563.RAHDmzu1tyTF0Q2Par_VShaxGZS-n5_u2NHXhhSGlU6CA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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" .
}