@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_head
{
this:
np:hasAssertion
dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_assertion
;
np:hasProvenance
dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_provenance
;
np:hasPublicationInfo
dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_assertion
a
np:Assertion
.
dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_provenance
a
np:Provenance
.
dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN8a302ba1bed12e71fdc6aa41275915d8
sio:SIO_000628
miriam-gene:1956
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_provenance
{
dgn-np:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_assertion
dcterms:description
"[Our data indicate that unlike NSCLC, EGFR kinase mutations are rare in unselected cases of SCCHN within the United States and are not linked to gefitinib or erlotinib responses in SCCHN.]. 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:16299242
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP523330.RA2P27gvHeLW3T-Mey54VmFHzIXdqEsDpO1LKzFItVkH0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:42+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}