@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8
> .
@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:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_head
{
this:
np:hasAssertion
dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_assertion
;
np:hasProvenance
dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_provenance
;
np:hasPublicationInfo
dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_assertion
a
np:Assertion
.
dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_provenance
a
np:Provenance
.
dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_assertion
{
miriam-gene:4157
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN68c19337adf982fae0318935ba5a0114
sio:SIO_000628
miriam-gene:4157
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_provenance
{
dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_assertion
dcterms:description
"[This study proposes the relevance of loss of function MC1R variants in the risk of melanoma in multiple primary melanoma cases with family history from areas with low melanoma incidence rate.]. 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:20539244
;
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:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:55+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" .
}