@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ
> .
@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:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_head
{
this:
np:hasAssertion
dgn-np:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_assertion
;
np:hasProvenance
dgn-np:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_assertion
a
np:Assertion
.
dgn-np:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_provenance
a
np:Provenance
.
dgn-np:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_assertion
{
miriam-gene:4893
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGN639f0eceb545b4b993cc02a871341903
sio:SIO_000628
miriam-gene:4893
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_provenance
{
dgn-np:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_assertion
dcterms:description
"[Our analysis of melanoma cell lines suggests that activating mutations in BRAF can occur simultaneously with inactivation of phosphatase and tensin homolog (PTEN), but neuroblastoma RAS (NRAS) mutations are not coincident.]. 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:16417231
;
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:NP318698.RAtp1LPSw4pWD0W87WHFYfNzCWVe2HOOtFiZmPpOxsJmQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:05+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" .
}