@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8
> .
@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:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_head
{
this:
np:hasAssertion
dgn-np:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_assertion
;
np:hasProvenance
dgn-np:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_provenance
;
np:hasPublicationInfo
dgn-np:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_assertion
a
np:Assertion
.
dgn-np:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_provenance
a
np:Provenance
.
dgn-np:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN90aabcb09a9531e0da16477427e92ce6
sio:SIO_000628
miriam-gene:2952
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_provenance
{
dgn-np:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_assertion
dcterms:description
"[The frequencies of the putatively high risk GSTT1 null genotype were not increased in the lung, oral or gastric cancer cases compared with controls but the frequency of this genotype was significantly increased (P = 0.0011, odds ratio = 1.88) in the colorectal cancer cases.]. 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:8625505
;
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:NP290682.RAxFPqvHDiqD4xCx92KRfUvdx6lgFkMFfScYhJnckd-X8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}