@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_head
{
this:
np:hasAssertion
dgn-np:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_assertion
;
np:hasProvenance
dgn-np:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_provenance
;
np:hasPublicationInfo
dgn-np:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_assertion
a
np:Assertion
.
dgn-np:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_provenance
a
np:Provenance
.
dgn-np:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0029456
a
ncit:C7057
.
dgn-gda:DGN216bc38b16563e09186c2734dfdff2a5
sio:SIO_000628
miriam-gene:64127
,
lld:C0029456
;
a
sio:SIO_001121
.
}
dgn-np:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_provenance
{
dgn-np:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_assertion
dcterms:description
"[These data suggests that the presence of any of the main NOD2 variants in CD is associated with osteoporosis and an age of onset dependent influence towards underweight, higher disease activity and a more intensive immunosuppressive therapy.]. 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:23635032
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP937548.RAa-AhefR0s6ifV_c--mUQ0Uksx2rdOqYfrsyAMlBd1PM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:12+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}