@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY
> .
@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:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_head
{
this:
np:hasAssertion
dgn-np:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_assertion
;
np:hasProvenance
dgn-np:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_provenance
;
np:hasPublicationInfo
dgn-np:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_assertion
a
np:Assertion
.
dgn-np:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_provenance
a
np:Provenance
.
dgn-np:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGNc3913ce168c144189f4d1ab2e1e20cf0
sio:SIO_000628
miriam-gene:2068
,
lld:C0001418
;
a
sio:SIO_001122
.
}
dgn-np:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_provenance
{
dgn-np:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_assertion
dcterms:description
"[Findings indicate that the Asp312Asn and Lys751Gln polymorphisms in the XPD locus are associated with the risk of lung Squamous Cell Carcinoma (SCC) but not lung adenocarcinoma or esophageal SCC in this Chinese population.]. 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:12579497
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP114370.RAwiJSIGx-fMqGrQRH4drA-6Q7TE4Kx1puGB5nQa_VyNY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:59+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" .
}