@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc
> .
@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:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_head
{
this:
np:hasAssertion
dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_assertion
;
np:hasProvenance
dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_provenance
;
np:hasPublicationInfo
dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_assertion
a
np:Assertion
.
dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_provenance
a
np:Provenance
.
dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_assertion
{
miriam-gene:6387
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN9936de86424ad695144130ab7dbc8595
sio:SIO_000628
miriam-gene:6387
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_provenance
{
dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_assertion
dcterms:description
"[Among CXC chemokines, single nucleotide polymorphisms (SNPs) in the CXCL8 and CXCL12 genes stand out, as they have alleles associated with many diseases such as asthma and human immunodeficiency virus (HIV), respectively.]. 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:17848170
;
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:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:44+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" .
}