@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q
> .
@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:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_head
{
this:
np:hasAssertion
dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_assertion
;
np:hasProvenance
dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_assertion
a
np:Assertion
.
dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_provenance
a
np:Provenance
.
dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_assertion
{
miriam-gene:729230
a
ncit:C16612
.
lld:C0002895
a
ncit:C7057
.
dgn-gda:DGN27447c8275fe80d72f1ac58a7fa22772
sio:SIO_000628
miriam-gene:729230
,
lld:C0002895
;
a
sio:SIO_001122
.
}
dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_provenance
{
dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_assertion
dcterms:description
"[In order to contribute to the identification of the genetic differences underlying this phenotypic diversity in SCD, we proposed to study the distribution of polymorphic variants of the genes encoding the chemokine receptors CCR2 and CCR5, as well as three polymorphisms in the NOS3 gene, in Brazilian SCD patients.]. 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:16305685
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}