@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo
> .
@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:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_head
{
this:
np:hasAssertion
dgn-np:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_assertion
;
np:hasProvenance
dgn-np:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_provenance
;
np:hasPublicationInfo
dgn-np:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_assertion
a
np:Assertion
.
dgn-np:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_provenance
a
np:Provenance
.
dgn-np:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_assertion
{
miriam-gene:999
a
ncit:C16612
.
lld:C0032927
a
ncit:C7057
.
dgn-gda:DGN0dbbfe9a7c51187f661fc0575c26dd12
sio:SIO_000628
miriam-gene:999
,
lld:C0032927
;
a
sio:SIO_001121
.
}
dgn-np:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_provenance
{
dgn-np:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_assertion
dcterms:description
"[This is the first study that indicates that CDH1 polymorphisms can contribute to the etiology of premalignant skin lesions in people chronically exposed to arsenic in drinking water, and that this gene may be a factor in individual susceptibility to cutaneous diseases.]. 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:22330421
;
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:NP484150.RAzEp1I1MicCGi8V49PS5Ojghhf68Yn3nd_OkZ44tkcpo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:49+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" .
}