@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU
> .
@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:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_head
{
this:
np:hasAssertion
dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_assertion
;
np:hasProvenance
dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_provenance
;
np:hasPublicationInfo
dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_assertion
a
np:Assertion
.
dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_provenance
a
np:Provenance
.
dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_assertion
{
miriam-gene:3127
a
ncit:C16612
.
lld:C0032026
a
ncit:C7057
.
dgn-gda:DGN05c56015a58a05f2f83709573284c59b
sio:SIO_000628
miriam-gene:3127
,
lld:C0032026
;
a
sio:SIO_001122
.
}
dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_provenance
{
dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_assertion
dcterms:description
"[We suggest that alleles DQB1*04 may be involved in the genetic susceptibility of PR based on the significant predominance of those alleles observed in the black PR patients. We also recommend that more studies are conducted on populations of other ethnic origins, preferentially with higher resolution techniques of DNA typing.]. 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:16405603
;
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:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:32+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" .
}