@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0
> .
@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:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_head
{
this:
np:hasAssertion
dgn-np:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_assertion
;
np:hasProvenance
dgn-np:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_provenance
;
np:hasPublicationInfo
dgn-np:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_assertion
a
np:Assertion
.
dgn-np:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_provenance
a
np:Provenance
.
dgn-np:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_assertion
{
miriam-gene:207
a
ncit:C16612
.
lld:C0007114
a
ncit:C7057
.
dgn-gda:DGNf26e60d06637f77ebdeddd37714ab89d
sio:SIO_000628
miriam-gene:207
,
lld:C0007114
;
a
sio:SIO_001121
.
}
dgn-np:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_provenance
{
dgn-np:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_assertion
dcterms:description
"[To determine the prevalence of AKT E17K mutations in melanoma, the most aggressive form of skin cancer, we analysed 137 human melanoma specimens and 65 human melanoma cell lines for the previously described activating mutation of AKT1, and for analogous mutations in AKT2 and AKT3.]. 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:18813315
;
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:NP784003.RAkpfC-0MUFdlJfdkkBo1BhF5Qv9_0OY_r-lhkVgq1SA0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:55+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" .
}