@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw
> .
@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:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_head
{
this:
np:hasAssertion
dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_assertion
;
np:hasProvenance
dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_provenance
;
np:hasPublicationInfo
dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_assertion
a
np:Assertion
.
dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_provenance
a
np:Provenance
.
dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_assertion
{
miriam-gene:3553
a
ncit:C16612
.
lld:C2827470
a
ncit:C7057
.
dgn-gda:DGN4950443553b7c16c8c3992c3cf87f25e
sio:SIO_000628
miriam-gene:3553
,
lld:C2827470
;
a
sio:SIO_001121
.
}
dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_provenance
{
dgn-np:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_assertion
dcterms:description
"[In a case-control study on the causes of deep venous thrombosis, the Leiden Thrombophilia Study (LETS), we genotyped 18 single nucleotide polymorphisms (SNPs) in IL1B, IL1RN, IL1R1, and IL1R2, enabling us to tag a total of 25 haplotype groups.]. 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:17413037
;
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:NP846830.RAzj7IN9lsHD5LquFnt7V-MhH4brsZ4eozPtv_qfuLqAw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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" .
}