@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM
> .
@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:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_head
{
this:
np:hasAssertion
dgn-np:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_assertion
;
np:hasProvenance
dgn-np:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_provenance
;
np:hasPublicationInfo
dgn-np:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_assertion
a
np:Assertion
.
dgn-np:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_provenance
a
np:Provenance
.
dgn-np:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_assertion
{
miriam-gene:5291
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN9de5e5c258c7a585b705938a91e276c8
sio:SIO_000628
miriam-gene:5291
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_provenance
{
dgn-np:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_assertion
dcterms:description
"[Mutations in the genes associated with the PI3K/AKT pathway including PI3K, AKT, RAS and PTEN, are infrequently found within head and neck squamous cell carcinoma and more specifically are rarely reported in oral squamous cell carcinoma (OSCC) cases.]. 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:21824802
;
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:NP576659.RA6CEflm_rorrRKSHyy1n1rsqo3Ws02uE8yI2JMw5VNKM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:47+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" .
}