@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M
> .
@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:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_head
{
this:
np:hasAssertion
dgn-np:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_assertion
;
np:hasProvenance
dgn-np:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_provenance
;
np:hasPublicationInfo
dgn-np:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_assertion
a
np:Assertion
.
dgn-np:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_provenance
a
np:Provenance
.
dgn-np:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_assertion
{
miriam-gene:1810
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN8f510304ea91c791e44d9997db3b698d
sio:SIO_000628
miriam-gene:1810
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_provenance
{
dgn-np:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_assertion
dcterms:description
"[For the Class II antigens, frequencies of DR4, DQ5, DQ6, DQ7 and DQ8 were increased while those for DR6 and DR1 were decreased in the patients with MS. HLA types DR15 and DR4 were present at higher frequencies in patients with a younger age at disease onset; DR15 also appeared more frequent in the female patients.]. 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:15327033
;
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:NP718732.RAQkRGGuTkStYb-Gr9zHjgxFespsTTgMZ6dE3rYC2Xa_M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:16+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" .
}