@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8
> .
@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:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_head
{
this:
np:hasAssertion
dgn-np:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_assertion
;
np:hasProvenance
dgn-np:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_provenance
;
np:hasPublicationInfo
dgn-np:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_assertion
a
np:Assertion
.
dgn-np:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_provenance
a
np:Provenance
.
dgn-np:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGNa4ac4513e1f9f411c548bc2b4b9fc103
sio:SIO_000628
miriam-gene:2068
,
lld:C0007137
;
a
sio:SIO_001122
.
}
dgn-np:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_provenance
{
dgn-np:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_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:NP99201.RACGm0fewwFmQ4jlywEnNQRjNozbHfZ7ii3ey8v5DvbO8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:50+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" .
}