@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU
> .
@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:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_head
{
this:
np:hasAssertion
dgn-np:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_assertion
;
np:hasProvenance
dgn-np:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_provenance
;
np:hasPublicationInfo
dgn-np:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_assertion
a
np:Assertion
.
dgn-np:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_provenance
a
np:Provenance
.
dgn-np:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C1321872
a
ncit:C7057
.
dgn-gda:DGN47bee6fd5afa616300d3888fbee27a69
sio:SIO_000628
miriam-gene:673
,
lld:C1321872
;
a
sio:SIO_001121
.
}
dgn-np:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_provenance
{
dgn-np:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_assertion
dcterms:description
"[Melanocytic lesions, including Spitz nevi (SN), common benign nevi (CBN) and cutaneous metastatic melanoma (CMM), were analyzed for activating mutations in NRAS, HRAS and BRAF oncogenes, which induce cellular proliferation via the MAP kinase pathway.]. 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:17518771
;
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:NP512812.RAJlOt7Oi6cw4MPfQwZP4qWD1U-ZgpPsFGvbLkhpUrQkU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}