@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY
> .
@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:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_head
{
this:
np:hasAssertion
dgn-np:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_assertion
;
np:hasProvenance
dgn-np:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_provenance
;
np:hasPublicationInfo
dgn-np:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_assertion
a
np:Assertion
.
dgn-np:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_provenance
a
np:Provenance
.
dgn-np:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_assertion
{
miriam-gene:7294
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN1a932ee7923cad681a0493572bf6dca0
sio:SIO_000628
miriam-gene:7294
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_provenance
{
dgn-np:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_assertion
dcterms:description
"[It is not known how to predict response in patients with squamous cell carcinoma of the head and neck (SCCHN), where EGFR TK mutations are less frequent and where response rates in unselected patients are disappointing.]. 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:19197951
;
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:NP813797.RAMFRd5Lxt7R9gAbZv5qeMDDc6TBq9fARsOztKdn0xxhY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:19+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" .
}