@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw
> .
@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:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_head
{
this:
np:hasAssertion
dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion
;
np:hasProvenance
dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance
;
np:hasPublicationInfo
dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion
a
np:Assertion
.
dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance
a
np:Provenance
.
dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0015773
a
ncit:C7057
.
dgn-gda:DGNb63840073cb08499bc1194bb3804e891
sio:SIO_000628
miriam-gene:3126
,
lld:C0015773
;
a
sio:SIO_001121
.
}
dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance
{
dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion
dcterms:description
"[Of the 83 patients, 61 (73%) possessed the DR4 allele and within this group we have investigated the relative frequencies of two DQ beta gene variants of DQw3, DQw7 and DQw8, one of which we had previously found to be raised in Felty's syndrome.]. 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:2571385
;
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:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_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" .
}