@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo
> .
@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:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_head
{
this:
np:hasAssertion
dgn-np:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_assertion
;
np:hasProvenance
dgn-np:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_provenance
;
np:hasPublicationInfo
dgn-np:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_assertion
a
np:Assertion
.
dgn-np:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_provenance
a
np:Provenance
.
dgn-np:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_assertion
{
miriam-gene:3815
a
ncit:C16612
.
lld:C0206736
a
ncit:C7057
.
dgn-gda:DGN5e1e69e85b090246686aca29ca38ce66
sio:SIO_000628
miriam-gene:3815
,
lld:C0206736
;
a
sio:SIO_001121
.
}
dgn-np:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_provenance
{
dgn-np:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_assertion
dcterms:description
"[The lack of BRAF, NRAS, GNAQ, and KIT mutations seems to support the notion that MNH may be distinct from conventional melanoma and from other dermal melanomas, such as malignant blue nevi and melanoma arising in congenital nevi.]. 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:21934481
;
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:NP670764.RAkSJ5iEVE-uu2wlXLjUOWrJCzit9l19u0vvEplCe_yuo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}