@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8
> .
@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:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_head
{
this:
np:hasAssertion
dgn-np:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_assertion
;
np:hasProvenance
dgn-np:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_provenance
;
np:hasPublicationInfo
dgn-np:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_assertion
a
np:Assertion
.
dgn-np:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_provenance
a
np:Provenance
.
dgn-np:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_assertion
{
miriam-gene:79823
a
ncit:C16612
.
lld:C0036220
a
ncit:C7057
.
dgn-gda:DGNd7d4712e0633003aef398cfe2958f3c8
sio:SIO_000628
miriam-gene:79823
,
lld:C0036220
;
a
sio:SIO_001121
.
}
dgn-np:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_provenance
{
dgn-np:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_assertion
dcterms:description
"[Thus, the induction of CAM expression could be an early event in the development of KS by recruiting leukocytes into KS lesions, thereby providing factors that could potentiate the development of KS.]. 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:7504714
;
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:NP571836.RAUCldPNHMkFGN0_vX0y1_SrNarZ5qW-Reuo_-T3uyof8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}