@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0
> .
@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:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_head
{
this:
np:hasAssertion
dgn-np:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_assertion
;
np:hasProvenance
dgn-np:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_provenance
;
np:hasPublicationInfo
dgn-np:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_assertion
a
np:Assertion
.
dgn-np:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_provenance
a
np:Provenance
.
dgn-np:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_assertion
{
miriam-gene:3105
a
ncit:C16612
.
lld:C0011615
a
ncit:C7057
.
dgn-gda:DGN61e9e058647a1f9213442cdb0ab0dbb1
sio:SIO_000628
miriam-gene:3105
,
lld:C0011615
;
a
sio:SIO_001121
.
}
dgn-np:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_provenance
{
dgn-np:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_assertion
dcterms:description
"[HLA A and B genotyping were practised for 53 atopic dermatitis patients and 76 healthy controls using the microlymphotoxicity complement dependent technique, while HLA DR and DQ genetyping were practised for only 20 patients with AD and all the controls by PCR-SSP method.]. 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:18236804
;
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:NP436389.RAzo1N696L9bm_9FRPlTHwnbuMRsLIa5r9-NH8USxVHN0130_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" .
}