@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc
> .
@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:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_head
{
this:
np:hasAssertion
dgn-np:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_assertion
;
np:hasProvenance
dgn-np:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_provenance
;
np:hasPublicationInfo
dgn-np:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_assertion
a
np:Assertion
.
dgn-np:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_provenance
a
np:Provenance
.
dgn-np:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGN07834913a09b50dafdf3f0ca97a2d47f
sio:SIO_000628
miriam-gene:1543
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_provenance
{
dgn-np:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_assertion
dcterms:description
"[Our findings suggested that CYP1A1 or GSTM1 variants may significantly modify the associations between level of serum trace metals (Cu, Zn, Se or Cr) and NSCLC, indicating the intriguing pathogenesis of lung cancer.]. 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:20638923
;
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:NP435858.RA3Ne8kMzdaMURy_yD0TMpwXX6wpY0vd-NjUHTvK7lduc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}