@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU
> .
@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:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_head
{
this:
np:hasAssertion
dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_assertion
;
np:hasProvenance
dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_provenance
;
np:hasPublicationInfo
dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_assertion
a
np:Assertion
.
dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_provenance
a
np:Provenance
.
dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_assertion
{
miriam-gene:6581
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGNafc1cdf583f036da67313befbc562f5c
sio:SIO_000628
miriam-gene:6581
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_provenance
{
dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_assertion
dcterms:description
"[Collectively, our data reveal that SP cells in the CNE-2 cell line not only possess the properties of cancer stem cells, but also have more mesenchymal cell characteristics which are associated with epithelial mesenchymal transition (EMT) and cancer cell invasion and metastasis.]. 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:22552840
;
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:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}