@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o
> .
@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:NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o130_head
{
this:
np:hasAssertion
dgn-np:NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o130_assertion
;
np:hasProvenance
dgn-np:NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o130_provenance
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np:hasPublicationInfo
dgn-np:NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o130_assertion
a
np:Assertion
.
dgn-np:NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o130_provenance
a
np:Provenance
.
dgn-np:NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:1591
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN8fb93fe29a3dcb93077f47afcdbb932a
sio:SIO_000628
miriam-gene:1591
,
lld:C0025202
;
a
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.
}
dgn-np:NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o130_provenance
{
dgn-np:NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o130_assertion
dcterms:description
"[In our hospital-based case-control study including 305 melanoma patients and 370 healthy controls single nucleotide polymorphisms in the genes CYP27B1 (rs4646536), CYP24A1 (rs927650), VDBP (rs1155563, rs7041), and VDR (rs757343, rs731236, rs2107301, rs7975232) were analyzed for their association with melanoma risk and prognosis.]. 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:22576141
;
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:NP457136.RAfFOeYHXn7X2Fpjqy_VVa8c7V2ryzHiORqdJ-bPfqe4o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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
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pav:authoredBy
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
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> , <
http://orcid.org/0000-0003-0169-8159
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
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"v2.1.0" .
}