@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU
> .
@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:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_head
{
this:
np:hasAssertion
dgn-np:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_assertion
;
np:hasProvenance
dgn-np:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_provenance
;
np:hasPublicationInfo
dgn-np:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_assertion
a
np:Assertion
.
dgn-np:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_provenance
a
np:Provenance
.
dgn-np:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_assertion
{
miriam-gene:3682
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN7af802569d73c82f875a0bd486d43d6d
sio:SIO_000628
miriam-gene:3682
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_provenance
{
dgn-np:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_assertion
dcterms:description
"[The aims of this research were to determine the number of chromosomal aberrations in peripheral blood lymphocytes and to evaluate the number of circulating lymphocytes with CD103, integrin expressed on intraepithelial lymphocytes and preserved in enteropathy-associated T-cell lymphoma, in patients with newly diagnosed Crohn's disease, celiac disease, and healthy controls.]. 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:23022983
;
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:NP227592.RACErJ_MFZ7Wcgvn9l5K7ujOCKEXf4yKH0Dgupq00d9VU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:06+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" .
}