@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw
> .
@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:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_head
{
this:
np:hasAssertion
dgn-np:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_assertion
;
np:hasProvenance
dgn-np:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_provenance
;
np:hasPublicationInfo
dgn-np:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_assertion
a
np:Assertion
.
dgn-np:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_provenance
a
np:Provenance
.
dgn-np:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_assertion
{
miriam-gene:5294
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNac1733eca74010945253edecb03267e1
sio:SIO_000628
miriam-gene:5294
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_provenance
{
dgn-np:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_assertion
dcterms: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:NP177598.RAdyEgeCF_aK-khW9XikcuwGmFcTlj0BnW8JapmN7ZKGw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}