@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk
> .
@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:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_head
{
this:
np:hasAssertion
dgn-np:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_assertion
;
np:hasProvenance
dgn-np:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_provenance
;
np:hasPublicationInfo
dgn-np:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_assertion
a
np:Assertion
.
dgn-np:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_provenance
a
np:Provenance
.
dgn-np:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_assertion
{
miriam-gene:8718
a
ncit:C16612
.
lld:C0340164
a
ncit:C7057
.
dgn-gda:DGNd12a39a2313faec3e9575f411df54a11
sio:SIO_000628
miriam-gene:8718
,
lld:C0340164
;
a
sio:SIO_001121
.
}
dgn-np:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_provenance
{
dgn-np:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_assertion
dcterms:description
"[The results not only substantiated the previous findings, but also showed that the virtual haplotype DR3.TNFalpha2 was significantly associated with Löfgren syndrome and that the virtual haplotype DR2.TNFalpha1 was noticeably although not significantly associated with the non-Löfgren patients.]. 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:11587099
;
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:NP413350.RAx9SYMk-CHFdEXMqRKcYcJYFkoVCW6oDyEmjuFQ2EkJk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}