@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ
> .
@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:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_head
{
this:
np:hasAssertion
dgn-np:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_assertion
;
np:hasProvenance
dgn-np:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_assertion
a
np:Assertion
.
dgn-np:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_provenance
a
np:Provenance
.
dgn-np:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGNc4f72fc9fb671655fbd4886624f4292a
sio:SIO_000628
miriam-gene:3133
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_provenance
{
dgn-np:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_assertion
dcterms:description
"[We have genotyped 14,436 nonsynonymous SNPs (nsSNPs) and 897 major histocompatibility complex (MHC) tag SNPs from 1,000 independent cases of ankylosing spondylitis (AS), autoimmune thyroid disease (AITD), multiple sclerosis (MS) and breast cancer (BC).]. 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:17952073
;
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:NP435425.RA54GEenBQnWep_HahpfwoSIkLC17V1JZpiWHl_Lr8nsQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}