@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls
> .
@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:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_head
{
this:
np:hasAssertion
dgn-np:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_assertion
;
np:hasProvenance
dgn-np:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_provenance
;
np:hasPublicationInfo
dgn-np:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_assertion
a
np:Assertion
.
dgn-np:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_provenance
a
np:Provenance
.
dgn-np:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0007570
a
ncit:C7057
.
dgn-gda:DGNfdc9601d3aadc5fd4ed60a6e6f76fa3a
sio:SIO_000628
miriam-gene:7124
,
lld:C0007570
;
a
sio:SIO_001122
.
}
dgn-np:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_provenance
{
dgn-np:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_assertion
dcterms:description
"[The TNFA -308 polymorphism and the polymorphism at the first intron of the LTA gene were typed in CD patients and healthy controls and the results were correlated with the presence of DQ2.]. 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:12439617
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP50192.RAZxuMOOZHMMq6_czoUTcx9dKIN_FQKbSR8iHVQahikls130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}