@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk
> .
@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:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_head
{
this:
np:hasAssertion
dgn-np:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_assertion
;
np:hasProvenance
dgn-np:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_provenance
;
np:hasPublicationInfo
dgn-np:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_assertion
a
np:Assertion
.
dgn-np:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_provenance
a
np:Provenance
.
dgn-np:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0220641
a
ncit:C7057
.
dgn-gda:DGN0390307bc9fc282bee5ed3cfcfcde116
sio:SIO_000628
miriam-gene:1956
,
lld:C0220641
;
a
sio:SIO_001121
.
}
dgn-np:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_provenance
{
dgn-np:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_assertion
dcterms:description
"[Our data indicate that an increased EGFR gene copy number is common in and associated with OSCC development in patients with OPLs expressing high EGFR, particularly OSCC developing at the site of a high-expression OPL; they also suggest that EGFR inhibitors may prevent oral cancer in patients with OPLs having an increased EGFR gene copy number.]. 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:20570883
;
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:NP422866.RA0IHbcdUXGX1pzp8EzbzYT8z8f1wOYUOHu0eSA7CVFWk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}