@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0
> .
@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:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_head
{
this:
np:hasAssertion
dgn-np:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_assertion
;
np:hasProvenance
dgn-np:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_provenance
;
np:hasPublicationInfo
dgn-np:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_assertion
a
np:Assertion
.
dgn-np:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_provenance
a
np:Provenance
.
dgn-np:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNed3fb1de690027554e592f0a49ec12e8
sio:SIO_000628
miriam-gene:1588
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_provenance
{
dgn-np:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_assertion
dcterms:description
"[To investigate if common variants of CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1 and CYP19A1 influence CRC risk we genotyped 2,575 CRC cases and 2,707 controls for 20 single nucleotide polymorphisms (SNPs) that have not previously been shown to have functional consequence within these genes.]. 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:17615053
;
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:NP668763.RAa8Amo-DL1v6SuKLKgXyLo2UNHFhpWMPtCWIm_tTqwf0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:44+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" .
}