@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo
> .
@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:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_head
{
this:
np:hasAssertion
dgn-np:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_assertion
;
np:hasProvenance
dgn-np:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_provenance
;
np:hasPublicationInfo
dgn-np:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_assertion
a
np:Assertion
.
dgn-np:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_provenance
a
np:Provenance
.
dgn-np:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0007114
a
ncit:C7057
.
dgn-gda:DGN6a9388ce31232821e9d946d434bccf94
sio:SIO_000628
miriam-gene:1029
,
lld:C0007114
;
a
sio:SIO_001121
.
}
dgn-np:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_provenance
{
dgn-np:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_assertion
dcterms:description
"[Cutaneous and ocular nevi, benign and malignant neoplasms of skin and other sites, brief skin cancer risk assessment tool risk classification for cutaneous melanoma, DNA sequencing of p16INK4a and p14ARF genes, and citations on familial uveal melanoma.]. 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:17207529
;
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:NP630305.RADv03fZzd-WQzmc69rHlH1ANMPibhljxQ4MhjyNPzKLo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:20+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" .
}