@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg
> .
@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:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_head
{
this:
np:hasAssertion
dgn-np:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_assertion
;
np:hasProvenance
dgn-np:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_provenance
;
np:hasPublicationInfo
dgn-np:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_assertion
a
np:Assertion
.
dgn-np:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_provenance
a
np:Provenance
.
dgn-np:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_assertion
{
miriam-gene:2767
a
ncit:C16612
.
lld:C0220633
a
ncit:C7057
.
dgn-gda:DGNacc92022953b5d4d002b662fe7da3633
sio:SIO_000628
miriam-gene:2767
,
lld:C0220633
;
a
sio:SIO_001121
.
}
dgn-np:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_provenance
{
dgn-np:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_assertion
dcterms:description
"[The recent identification of frequent activating mutations in GNAQ or GNA11 in uveal melanoma provides an opportunity to better understand the pathogenesis of this melanoma subtype and to develop rational therapeutics to target the cellular effects mediated by these mutations.]. 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:22236444
;
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:NP238144.RATJOBErkm0bFBZGJvb-WDSDHTAbgfvwlYB8kFwved_Hg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}