@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E
> .
@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:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_head
{
this:
np:hasAssertion
dgn-np:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_assertion
;
np:hasProvenance
dgn-np:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_assertion
a
np:Assertion
.
dgn-np:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_provenance
a
np:Provenance
.
dgn-np:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_assertion
{
miriam-gene:26191
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGNfdfab0d5b321dec41e7c39800f17eb6f
sio:SIO_000628
miriam-gene:26191
,
lld:C0009324
;
a
sio:SIO_001121
.
}
dgn-np:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_provenance
{
dgn-np:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_assertion
dcterms:description
"[No significant association was found between the frequencies of genotypes of the PTPN22 gene with either the clinical features such as sex, age, age at disease onset, and extent of colitis, or the production of serological markers (anti-Saccharomyces cerevisiae antibody in CD and perinuclear anti-neutrophil cytoplasmic antibody in UC).]. 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:20101775
;
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:NP570895.RANiIIqN58izpj3tiEDdN1QFBL67P8vrXrzAxiXwNou3E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}