@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q
> .
@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:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_head
{
this:
np:hasAssertion
dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_assertion
;
np:hasProvenance
dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_assertion
a
np:Assertion
.
dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_provenance
a
np:Provenance
.
dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_assertion
{
miriam-gene:4893
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNdbef0785add4a936797be4c16e12f386
sio:SIO_000628
miriam-gene:4893
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_provenance
{
dgn-np:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_assertion
dcterms:description
"[This review will focus on mutations in genes encoding proteins that play a role in the MAPK pathway and that have been implicated in melanoma biology, such as BRAF, NRAS, and MEK (MAPK kinase), and detail the current understanding of their role in melanoma progression from a molecular biology perspective.]. 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:23752084
;
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:NP163351.RAlsUhlrcSvO9MSiESiG232eYvSyHInn3VNG29p_za43Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}