@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA130_assertion
;
np:hasProvenance
dgn-np:NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA130_provenance
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np:hasPublicationInfo
dgn-np:NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA130_assertion
a
np:Assertion
.
dgn-np:NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA130_provenance
a
np:Provenance
.
dgn-np:NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA130_assertion
{
miriam-gene:4331
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGNa383142bf414210c0a04ab82b46b7346
sio:SIO_000628
miriam-gene:4331
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA130_provenance
{
dgn-np:NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA130_assertion
dcterms:description
"[To test whether the genetic variants of CAK genes modify the risk of lung cancer, we compared the manifestation of 25 single nucleotide polymorphisms (SNPs) and the haplotypes of Cdk7, MAT1 and cyclin H between 500 patients with lung cancer and 517 healthy 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:17707548
;
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 .
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dgn-np:NP487599.RAFF0vPFlh0qVZUYEg1AlpF1kJKMLgiCsWU6LcXgHE5kA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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
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dgn-void:disgenetrdf
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"v2.1.0" .
}