@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c
> .
@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:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_head
{
this:
np:hasAssertion
dgn-np:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_assertion
;
np:hasProvenance
dgn-np:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_provenance
;
np:hasPublicationInfo
dgn-np:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_assertion
a
np:Assertion
.
dgn-np:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_provenance
a
np:Provenance
.
dgn-np:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_assertion
{
miriam-gene:7097
a
ncit:C16612
.
lld:C0275551
a
ncit:C7057
.
dgn-gda:DGNdf2481373ef56a22cd0c22390117d40b
sio:SIO_000628
miriam-gene:7097
,
lld:C0275551
;
a
sio:SIO_001121
.
}
dgn-np:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_provenance
{
dgn-np:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_assertion
dcterms:description
"[Since they may contribute to susceptibility to spontaneous bacterial peritonitis (SBP), we studied the effects of TLR2 gene variants on susceptibility for SBP in relation to the previously reported NOD2 alleles.]. 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:21356257
;
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:NP510698.RAUNHYX_a1fKm6nkd4CotJ44haLxc_yaXdgPUwtYXOS8c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}