@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_head
{
this:
np:hasAssertion
dgn-np:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_assertion
;
np:hasProvenance
dgn-np:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_assertion
a
np:Assertion
.
dgn-np:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_provenance
a
np:Provenance
.
dgn-np:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_assertion
{
miriam-gene:2767
a
ncit:C16612
.
lld:C0206739
a
ncit:C7057
.
dgn-gda:DGN8ae05f776ba6bf7e5368a75e5fb252be
sio:SIO_000628
miriam-gene:2767
,
lld:C0206739
;
a
sio:SIO_001121
.
}
dgn-np:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_provenance
{
dgn-np:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_assertion
dcterms:description
"[The presence of HRAS mutations and absence of GNAQ or GNA11 mutations in deep penetrating nevi suggests classification of these unusual nevi within the Spitz nevus category of melanocytic tumors, rather than the blue nevus category.]. 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:23599145
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1070734.RAi08ZPC6Fod_0RGUMBXnKIQcJphXseAWYTGYdft3pRjk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:51+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}