@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0
> .
@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:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_head
{
this:
np:hasAssertion
dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_assertion
;
np:hasProvenance
dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_provenance
;
np:hasPublicationInfo
dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_assertion
a
np:Assertion
.
dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_provenance
a
np:Provenance
.
dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0205851
a
ncit:C7057
.
dgn-gda:DGN451e818a9d85cca351c76db36de9b6cd
sio:SIO_000628
miriam-gene:1956
,
lld:C0205851
;
a
sio:SIO_001121
.
}
dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_provenance
{
dgn-np:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_assertion
dcterms:description
"[These results suggest that overexpression of EGFR protein and increased copy number or amplification of the EGFR gene occur relatively frequently in primary TGCTs, and may play roles in the formation of invasive cancer and in the progression, especially morphological evolution, of tumors.]. 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:20608935
;
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:NP337937.RAvfhiwqlYMJ1NDZXnoL3XGaM9oTdv3FW1VmvvM_hwix0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}