@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ
> .
@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:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_head
{
this:
np:hasAssertion
dgn-np:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_assertion
;
np:hasProvenance
dgn-np:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_assertion
a
np:Assertion
.
dgn-np:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_provenance
a
np:Provenance
.
dgn-np:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_assertion
{
miriam-gene:1800
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN5e88aa81be158d723ca02787015bf587
sio:SIO_000628
miriam-gene:1800
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_provenance
{
dgn-np:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_assertion
dcterms:description
"[NOD2 is an intracellular receptor for the bacterial cell wall component muramyl dipeptide (MDP), and variants of NOD2 are associated with chronic inflammatory diseases of barrier organs (e.g., Crohn's disease, asthma, and atopic eczema).]. 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:21335489
;
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:NP913175.RAoJtV88efs3XBg0quEfS8Tzk80wZUCrzMaaJWBLUoMTQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:20+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" .
}