@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4
> .
@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:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_head
{
this:
np:hasAssertion
dgn-np:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_assertion
;
np:hasProvenance
dgn-np:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_provenance
;
np:hasPublicationInfo
dgn-np:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_assertion
a
np:Assertion
.
dgn-np:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_provenance
a
np:Provenance
.
dgn-np:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_assertion
{
miriam-gene:4893
a
ncit:C16612
.
lld:C0700095
a
ncit:C7057
.
dgn-gda:DGNd859b2ccc28507fb0d2fcadfb0c51d6d
sio:SIO_000628
miriam-gene:4893
,
lld:C0700095
;
a
sio:SIO_001121
.
}
dgn-np:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_provenance
{
dgn-np:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_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:NP477578.RAHJ-3xT5jQhgBEIkFtMH5_EJlRM5D7Pbi5llwrpSVFh4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:46+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" .
}