@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8
> .
@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:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_head
{
this:
np:hasAssertion
dgn-np:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_assertion
;
np:hasProvenance
dgn-np:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_provenance
;
np:hasPublicationInfo
dgn-np:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_assertion
a
np:Assertion
.
dgn-np:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_provenance
a
np:Provenance
.
dgn-np:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_assertion
{
miriam-gene:3109
a
ncit:C16612
.
lld:C0409980
a
ncit:C7057
.
dgn-gda:DGN6c4c46bf910ff7be0cb86170ebd37e66
sio:SIO_000628
miriam-gene:3109
,
lld:C0409980
;
a
sio:SIO_001121
.
}
dgn-np:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_provenance
{
dgn-np:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_assertion
dcterms:description
"[HLA-DMA and DMB polymorphisms were genotyped by polymerase chain reaction combined with restriction enzyme digestion in 51 white patients with primary antiphospholipid syndrome (APS), 82 with systemic lupus erythematosus (SLE) (42 with APS and 40 without APS), and 109 healthy white controls.]. 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:15547089
;
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:NP779890.RA4gaRrzEgHnMl0Rp02LDpX2KwfNot89Q8_sqjp76fnX8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:52+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" .
}