@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o
> .
@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:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_head
{
this:
np:hasAssertion
dgn-np:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_assertion
;
np:hasProvenance
dgn-np:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_provenance
;
np:hasPublicationInfo
dgn-np:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_assertion
a
np:Assertion
.
dgn-np:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_provenance
a
np:Provenance
.
dgn-np:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN7b367f909f1ce401c64b8ebcd1be3961
sio:SIO_000628
miriam-gene:1956
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_provenance
{
dgn-np:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_assertion
dcterms:description
"[Further, large scale automated alignment of sequencing are unlikely to identify EGFRvIII and an assay specifically designed to detect EGFRvIII may be necessary to detect this altered form of EGFR in HNSCC 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:25658924
;
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:NP1261708.RAzvtY9nwnxaWU6XLmEyfAH1g0NCrf1LfaUHMcVmuq57o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:18+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" .
}