@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E
> .
@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:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_head
{
this:
np:hasAssertion
dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_assertion
;
np:hasProvenance
dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_provenance
;
np:hasPublicationInfo
dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_assertion
a
np:Assertion
.
dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_provenance
a
np:Provenance
.
dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0546837
a
ncit:C7057
.
dgn-gda:DGN0959a2081e2172d6a9dcabb923125bc7
sio:SIO_000628
miriam-gene:1543
,
lld:C0546837
;
a
sio:SIO_001122
.
}
dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_provenance
{
dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_assertion
dcterms:description
"[There were no significant differences in the frequency distribution of CYP1A1 polymorphisms between esophageal cancer patients and healthy controls although the frequency of CYP1A1 with at least one allele of Val showed slightly higher in individuals with esophageal 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:11860825
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}