@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU
> .
@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:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_head
{
this:
np:hasAssertion
dgn-np:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_assertion
;
np:hasProvenance
dgn-np:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_provenance
;
np:hasPublicationInfo
dgn-np:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_assertion
a
np:Assertion
.
dgn-np:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_provenance
a
np:Provenance
.
dgn-np:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_assertion
{
miriam-gene:3570
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN87d9f810033d7e44221d237fe411fe0b
sio:SIO_000628
miriam-gene:3570
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_provenance
{
dgn-np:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_assertion
dcterms:description
"[Although a common, non-synonymous variant in the IL-6 receptor gene (IL6R Asp358Ala; rs2228145 A>C) is associated with the risk of several common diseases, with the 358Ala allele conferring protection from coronary heart disease (CHD), rheumatoid arthritis (RA), atrial fibrillation (AF), abdominal aortic aneurysm (AAA), and increased susceptibility to asthma, the variant's effect on IL-6 signaling is not known.]. 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:23593036
;
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:NP432161.RADCuEAGiyMnJdAACEN7bw3fA2oZRB5d7SJNWZdfwtZSU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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" .
}