@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0
> .
@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:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_head
{
this:
np:hasAssertion
dgn-np:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_assertion
;
np:hasProvenance
dgn-np:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_provenance
;
np:hasPublicationInfo
dgn-np:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_assertion
a
np:Assertion
.
dgn-np:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_provenance
a
np:Provenance
.
dgn-np:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_assertion
{
miriam-gene:23495
a
ncit:C16612
.
lld:C0333559
a
ncit:C7057
.
dgn-gda:DGN39d63bcc2053824ee5396c1fbdf95601
sio:SIO_000628
miriam-gene:23495
,
lld:C0333559
;
a
sio:SIO_001121
.
}
dgn-np:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_provenance
{
dgn-np:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_assertion
dcterms:description
"[When patients were categorized according to the OCSP classification, it turned out that significant (p=0.002) decrease in TNF2 allele frequency (0.065) was restricted to the patients with lacunar infarct (LACI) whereas the frequency of the TNF2 alleles in patients with the other three subtypes (TACI, PACI, and POCI) did not significantly differ from that in 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:16473522
;
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:NP815035.RA2k6Ti1vqwggCQTzhBdIbbDImsUKQbPxj2gjSxmn4EX0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:19+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" .
}