@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g
> .
@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:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_head
{
this:
np:hasAssertion
dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_assertion
;
np:hasProvenance
dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_provenance
;
np:hasPublicationInfo
dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_assertion
a
np:Assertion
.
dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_provenance
a
np:Provenance
.
dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_assertion
{
miriam-gene:3106
a
ncit:C16612
.
lld:C0001824
a
ncit:C7057
.
dgn-gda:DGN895d6c25120df0a8d6a204da386f4213
sio:SIO_000628
miriam-gene:3106
,
lld:C0001824
;
a
sio:SIO_001121
.
}
dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_provenance
{
dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_assertion
dcterms:description
"[The results obtained revealed significant differences between the agranulocytosis patients and the healthy population in the human lymphocyte antigen (HLA) allele frequencies, and in the degree and the frequency of chromosome aberrations.]. 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:8845862
;
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:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}