@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU
> .
@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:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_head
{
this:
np:hasAssertion
dgn-np:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_assertion
;
np:hasProvenance
dgn-np:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_provenance
;
np:hasPublicationInfo
dgn-np:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_assertion
a
np:Assertion
.
dgn-np:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_provenance
a
np:Provenance
.
dgn-np:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0034069
a
ncit:C7057
.
dgn-gda:DGN976664b67108597f4899ed0ee278ddb0
sio:SIO_000628
miriam-gene:4204
,
lld:C0034069
;
a
sio:SIO_001121
.
}
dgn-np:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_provenance
{
dgn-np:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_assertion
dcterms:description
"[Our data clearly suggest the existence of two independent signals within the Xq28 region, one located in IRAK1 related to PF and another in MECP2 related to diffuse cutaneous SSc, indicating that both genes may have an impact on the clinical outcome of the disease.]. 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:23444193
;
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:NP798520.RAROFVdk34zld0S-opjQdEs-Su1XGYiKV-7V2cXTLkcnU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}