@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE130_assertion
;
np:hasProvenance
dgn-np:NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE130_provenance
;
np:hasPublicationInfo
dgn-np:NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE130_assertion
a
np:Assertion
.
dgn-np:NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE130_provenance
a
np:Provenance
.
dgn-np:NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE130_assertion
{
miriam-gene:3176
a
ncit:C16612
.
lld:C0272285
a
ncit:C7057
.
dgn-gda:DGN60cb0333854ad2e1c3c68112c188e2a9
sio:SIO_000628
miriam-gene:3176
,
lld:C0272285
;
a
sio:SIO_001121
.
}
dgn-np:NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE130_provenance
{
dgn-np:NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE130_assertion
dcterms:description
"[Case-control association study of all haplotype tagging and four previously reported DAO SNPs and one HNMT Single nucleotide polymorphism with symptoms of HIT and DAO serum activity in 484 German individuals including 285 patients with clinical symptoms of HIT and 199 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:21488903
;
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:NP925260.RATrJHn92OQhSjsXpTaLvTlT3e2RkxPPW5kB2clYyXImE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
}