@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww
> .
@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:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_head
{
this:
np:hasAssertion
dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_assertion
;
np:hasProvenance
dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_provenance
;
np:hasPublicationInfo
dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_assertion
a
np:Assertion
.
dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_provenance
a
np:Provenance
.
dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_assertion
{
miriam-gene:112744
a
ncit:C16612
.
lld:C0004364
a
ncit:C7057
.
dgn-gda:DGN00ff5cae758ea185aaf8cd4603e37531
sio:SIO_000628
miriam-gene:112744
,
lld:C0004364
;
a
sio:SIO_001121
.
}
dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_provenance
{
dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_assertion
dcterms:description
"[Among IL-17 families, IL-17A and IL-17F share amino acid sequence similarity and bind to IL-17R type A. IL-17 signaling is implicated in the pathogenesis of various autoimmune diseases, but its role in the regulatory mechanism of extracellular matrix expression and its contribution to the phenotype of systemic sclerosis (SSc) both remain to be elucidated.]. 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:22403442
;
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:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:55+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
<
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> , <
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
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}