@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk
> .
@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:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_head
{
this:
np:hasAssertion
dgn-np:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_assertion
;
np:hasProvenance
dgn-np:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_provenance
;
np:hasPublicationInfo
dgn-np:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_assertion
a
np:Assertion
.
dgn-np:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_provenance
a
np:Provenance
.
dgn-np:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_assertion
{
miriam-gene:5176
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNdf1a7c1d7e870fe587520bfab54855a0
sio:SIO_000628
miriam-gene:5176
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_provenance
{
dgn-np:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_assertion
dcterms:description
"[Our results show that loss of PEDF enables melanoma cells to acquire an invasive phenotype and, therefore, modulation of this multifunctional factor could be critical for the malignant progression of human melanoma.]. 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:19767774
;
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:NP803269.RAOQS7B5LAnknSiTYx2t8fJny48TzaNMiFyphelSyFbJk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}