@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA
> .
@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 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:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_head
{
this:
np:hasAssertion
dgn-np:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_assertion
;
np:hasProvenance
dgn-np:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_provenance
;
np:hasPublicationInfo
dgn-np:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_assertion
a
np:Assertion
.
dgn-np:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_provenance
a
np:Provenance
.
dgn-np:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_assertion
{
miriam-gene:5900
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN41f4139fd9d3a0893d760714dc5b5461
sio:SIO_000628
miriam-gene:5900
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_provenance
{
dgn-np:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_assertion
dct:description
"[An example is RAS, which is frequently mutated in cancer and contributes to initiation and maintenance of the disease by constitutive signal transduction through protein interaction with effector proteins, like PI3K, RAF and RALGDS.]. 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:17568777
;
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:NP355802.RABe7Zrvolkqjud0Q-UKxSQKN2Jyb5qIYP_KfHEtA1RWA130_publicationInfo
{
this:
dct:created
"2014-10-02T12:35:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}