@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg
> .
@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:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_head
{
this:
np:hasAssertion
dgn-np:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_assertion
;
np:hasProvenance
dgn-np:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_provenance
;
np:hasPublicationInfo
dgn-np:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_assertion
a
np:Assertion
.
dgn-np:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_provenance
a
np:Provenance
.
dgn-np:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_assertion
{
miriam-gene:3057
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNef9b3cb25fcf7160a0846448c52cbaf0
sio:SIO_000628
miriam-gene:3057
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_provenance
{
dgn-np:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_assertion
dcterms:description
"[In conclusion, our results show without ambiguity that in South European populations, MC1R RHC and SCL45A2 p.Phe374Leu variants are strong melanoma risk predictors, notably in those individuals who would not be identified as high risk based on their phenotypes or exposures alone.]. 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:22464347
;
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:NP922221.RAqCdE1_Z1zt2YWQvOeUXjrmgg_WW6zrCGIrFqLC2i6Rg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}