@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc
> .
@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:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_head
{
this:
np:hasAssertion
dgn-np:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_assertion
;
np:hasProvenance
dgn-np:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_provenance
;
np:hasPublicationInfo
dgn-np:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_assertion
a
np:Assertion
.
dgn-np:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_provenance
a
np:Provenance
.
dgn-np:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_assertion
{
miriam-gene:6387
a
ncit:C16612
.
lld:C0019829
a
ncit:C7057
.
dgn-gda:DGN424f1704de3df586fc041f2ad5e66139
sio:SIO_000628
miriam-gene:6387
,
lld:C0019829
;
a
sio:SIO_001121
.
}
dgn-np:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_provenance
{
dgn-np:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_assertion
dcterms:description
"[No or only very faint signals were obtained in HL for CXCL12, CCL7 and CCL8, but CXCL10, CCL5, CCL13, CCL17 and CCL22 were highly or differentially expressed in HL cell lines and tissues.]. 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:12115499
;
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:NP596373.RA_YsoB_LxuCBdrFfUCvUUzYO3xT_FEczvHvXkLTNCrQc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:58+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" .
}