@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_head
{
this:
np:hasAssertion
dgn-np:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_assertion
;
np:hasProvenance
dgn-np:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_provenance
;
np:hasPublicationInfo
dgn-np:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_assertion
a
np:Assertion
.
dgn-np:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_provenance
a
np:Provenance
.
dgn-np:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGNd134377ef051e5a891b3a2f742bd6fbe
sio:SIO_000628
miriam-gene:1565
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_provenance
{
dgn-np:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_assertion
dcterms:description
"[When we examined the associations between several single-nucleotide polymorphisms and ESCC in those with and without FHC, the associations of variant genotypes in cytochrome P450 (CYP) 2C19 and CYP2D6 and the wild genotype of CYP2E1 with ESCC were much stronger in those with FHC.]. 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:26125444
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1289090.RAvfuDhFZzKMLngfRnqX6d-0S5YjOIev8N5QdC5Do1E9k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:30+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}