@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4
> .
@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:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_head
{
this:
np:hasAssertion
dgn-np:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_assertion
;
np:hasProvenance
dgn-np:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_provenance
;
np:hasPublicationInfo
dgn-np:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_assertion
a
np:Assertion
.
dgn-np:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_provenance
a
np:Provenance
.
dgn-np:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_assertion
{
miriam-gene:3034
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNfc4a03cd428a4f63829b47ecf670377a
sio:SIO_000628
miriam-gene:3034
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_provenance
{
dgn-np:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_assertion
dcterms:description
"[We tested the hypothesis that genetic variation in the histidase gene (HAL), which catalyzes the formation of UCA in the skin, modifies risk of basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) in a population-based study (914 BCC, 702 SCC and 848 controls).]. 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:18641401
;
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:NP889002.RAlBO6fqStowo8Gct8BTeNdz1z1KCcWr-WkfIAtJenky4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:06+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" .
}