@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc
> .
@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:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_head
{
this:
np:hasAssertion
dgn-np:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_assertion
;
np:hasProvenance
dgn-np:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_provenance
;
np:hasPublicationInfo
dgn-np:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_assertion
a
np:Assertion
.
dgn-np:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_provenance
a
np:Provenance
.
dgn-np:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0003615
a
ncit:C7057
.
dgn-gda:DGNeb51b0d04668a48773df374b1f6b614a
sio:SIO_000628
miriam-gene:7124
,
lld:C0003615
;
a
sio:SIO_001122
.
}
dgn-np:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_provenance
{
dgn-np:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_assertion
dcterms:description
"[ Polymorphism in the IL-6 gene was associated with the severity of appendicitis, even after adjustment for duration of symptoms. The risk for developing appendiceal perforation or gangrene may be determined, in part, by variation in the IL-6 gene.]. 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:15273551
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP50055.RA2igopCB7NbaaPhzP0lofBZTnlMEkPUwanvJdldilwRc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}