@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08
> .
@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:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_head
{
this:
np:hasAssertion
dgn-np:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_assertion
;
np:hasProvenance
dgn-np:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_provenance
;
np:hasPublicationInfo
dgn-np:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_assertion
a
np:Assertion
.
dgn-np:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_provenance
a
np:Provenance
.
dgn-np:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN6aafdb6d7d253175813b26808ebdf65d
sio:SIO_000628
miriam-gene:1956
,
lld:C0007137
;
a
sio:SIO_001123
.
}
dgn-np:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_provenance
{
dgn-np:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_assertion
dcterms:description
"[heterozygous and synonymous transition of the EGFR gene and low EGFR expression levels of mRNA and protein in squamous cell carcinomas of the head and neck (SCCHN) may be reliable predictors of high sensitivity in SCCHN patients to gefitinib.]. 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:18097577
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP99085.RAWtpN3JyrRhuKTwwX6xDllovWE4MHfb7HfJ6_mD3RB08130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:50+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" .
}