@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk
> .
@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:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_head
{
this:
np:hasAssertion
dgn-np:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_assertion
;
np:hasProvenance
dgn-np:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_provenance
;
np:hasPublicationInfo
dgn-np:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_assertion
a
np:Assertion
.
dgn-np:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_provenance
a
np:Provenance
.
dgn-np:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGNd83ff58231bfe1f4a766abde7ccfd805
sio:SIO_000628
miriam-gene:673
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_provenance
{
dgn-np:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_assertion
dcterms:description
"[Although mutations in the downstream components of the EGFR signaling pathway, including KRAS, BRAF and PIK3CA, have been reported in numerous cancers, extensive mutation and copy number analysis of these genes in clinical samples has not been performed for head and neck squamous cell carcinoma (HNSCC).]. 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:22994622
;
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:NP725794.RAE_9H-xMW4L5ayIFJmptRnqIl3iIR-3N6X1GN1oeSnsk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}