@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_head
{
this:
np:hasAssertion
dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_assertion
a
np:Assertion
.
dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_provenance
a
np:Provenance
.
dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:1312
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGN519e3436dd2f8eae72d6d02b56f68b88
sio:SIO_000628
miriam-gene:1312
,
lld:C0007131
;
a
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.
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dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_provenance
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dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_assertion
dcterms:description
"[When we corrected for multiple testing using these statistical tools, three novel associations of NSCLC risk with SNPs in the CYP1B1 (Arg48Gly), COMT (Val158Met) and GSTT2 (Met139Ile) genes were found noteworthy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:18258609
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:41+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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pav:version
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