@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0
> .
@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:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_head
{
this:
np:hasAssertion
dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_assertion
;
np:hasProvenance
dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_provenance
;
np:hasPublicationInfo
dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_assertion
a
np:Assertion
.
dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_provenance
a
np:Provenance
.
dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_assertion
{
miriam-gene:10200
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN0252faf4a3a9ae370948a64ddf0d3dd1
sio:SIO_000628
miriam-gene:10200
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_provenance
{
dgn-np:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_assertion
dcterms:description
"[We found that the frequencies of GSTP1 genotypes based on the Ile105 and Val105-expressing alleles and CCND1 AA, AG, GG genotypes were similar in MPP and SPP cases and that there were no significant associations between GSTP1 or CCND1 genotypes and BCC numbers in the total or SPP groups.]. 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:10975609
;
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:NP549450.RACDn9v9dcQOImstTN3GAwFDBMRdT36EZCSpV34WE-_D0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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" .
}