@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE
> .
@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:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_head
{
this:
np:hasAssertion
dgn-np:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_assertion
;
np:hasProvenance
dgn-np:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_provenance
;
np:hasPublicationInfo
dgn-np:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_assertion
a
np:Assertion
.
dgn-np:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_provenance
a
np:Provenance
.
dgn-np:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0346360
a
ncit:C7057
.
dgn-gda:DGNe951e969eb2d0085af2beabc777e7ec5
sio:SIO_000628
miriam-gene:673
,
lld:C0346360
;
a
sio:SIO_001121
.
}
dgn-np:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_provenance
{
dgn-np:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_assertion
dcterms:description
"[To gain a better understanding of the molecular events leading to the development of conjunctival melanocytic lesions and conjunctival melanoma, this study was conducted to investigate the presence of T1799A BRAF oncogenic mutation in these lesions.]. 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:16123397
;
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:NP568913.RAcZNp2jLrkpqy1kcRQUkcpn_5TIrCUdcx0kfzhrEE2UE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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" .
}