@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU
> .
@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:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_head
{
this:
np:hasAssertion
dgn-np:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_assertion
;
np:hasProvenance
dgn-np:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_provenance
;
np:hasPublicationInfo
dgn-np:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_assertion
a
np:Assertion
.
dgn-np:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_provenance
a
np:Provenance
.
dgn-np:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_assertion
{
miriam-gene:4193
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGNaac295a895ebbddc2496277f0b6b564c
sio:SIO_000628
miriam-gene:4193
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_provenance
{
dgn-np:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_assertion
dcterms:description
"[The results thus demonstrate that the MDM2 SNP309 TT rather than the GG genotype is associated with increased risk of lung cancer in this population, suggesting that other mechanisms independent of increased MDM2 levels can influence cancer susceptibility.]. 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:20219101
;
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:NP331858.RA6pI9SaEgrE1svKuXhdheaXTfvpXh_W8bPyLIyC-kEeU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:15+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" .
}