@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI
> .
@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:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_head
{
this:
np:hasAssertion
dgn-np:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_assertion
;
np:hasProvenance
dgn-np:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_provenance
;
np:hasPublicationInfo
dgn-np:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_assertion
a
np:Assertion
.
dgn-np:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_provenance
a
np:Provenance
.
dgn-np:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C1704429
a
ncit:C7057
.
dgn-gda:DGN9207b5edc3154ff1bb0aed31d2756671
sio:SIO_000628
miriam-gene:1956
,
lld:C1704429
;
a
sio:SIO_001121
.
}
dgn-np:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_provenance
{
dgn-np:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_assertion
dcterms:description
"[A proteomic approach was used to generate differential protein expression maps of fetal human astrocytes (FHA), human glioblastoma cell lines U87MG and U87MG expressing type III EGFR deletion (U87MGdeltaEGFR) that confers high malignancy to tumor cells.]. 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:12655603
;
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:NP215924.RA53bcwzwQqsplAMRCL8so9-5PAGF1uA7muPUkJtN_ZGI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}