@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y
> .
@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:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_head
{
this:
np:hasAssertion
dgn-np:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_assertion
;
np:hasProvenance
dgn-np:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_assertion
a
np:Assertion
.
dgn-np:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_provenance
a
np:Provenance
.
dgn-np:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_assertion
{
miriam-gene:4671
a
ncit:C16612
.
lld:C0004623
a
ncit:C7057
.
dgn-gda:DGNd9d20d6a084bbc517ed2dda8dd8e22e6
sio:SIO_000628
miriam-gene:4671
,
lld:C0004623
;
a
sio:SIO_001121
.
}
dgn-np:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_provenance
{
dgn-np:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_assertion
dcterms:description
"[Notably, genetic variation in the genes encoding the NOD proteins NOD2, cryopyrin and CIITA (MHC class II transactivator) in humans and Naip5 (neuronal apoptosis inhibitory protein 5) in mice is associated with inflammatory disease or increased susceptibility to bacterial infections.]. 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:12766759
;
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:NP698952.RAwjWQoqDX7ju1_OBqi67oxfVYqwcJ12FgLtuJqD1lg5Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:05+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" .
}