@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs
> .
@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:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_head
{
this:
np:hasAssertion
dgn-np:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_assertion
;
np:hasProvenance
dgn-np:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_provenance
;
np:hasPublicationInfo
dgn-np:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_assertion
a
np:Assertion
.
dgn-np:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_provenance
a
np:Provenance
.
dgn-np:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0039103
a
ncit:C7057
.
dgn-gda:DGN2e2850cf1ea4c8a1fa7aa19004d6900d
sio:SIO_000628
miriam-gene:2099
,
lld:C0039103
;
a
sio:SIO_001121
.
}
dgn-np:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_provenance
{
dgn-np:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_assertion
dcterms:description
"[No significant differences were observed between the patients carrying the CCR5 delta 32 allele and those homozygous for the normal CCR5 allele when we compared sex, presence of distal synovitis and systemic signs and/or symptoms, initial and cumulative prednisone dose, duration of therapy, ESR at diagnosis, frequency of relapse/recurrence and RANTES serum levels at diagnosis and after 6 months of corticosteroids.]. 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:11072599
;
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:NP714828.RAI9UBW1Damgdv-gCxlvTZUzsmnV_Lknv4Iu3xFaF8KBs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:14+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" .
}