@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE
> .
@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:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_head
{
this:
np:hasAssertion
dgn-np:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_assertion
;
np:hasProvenance
dgn-np:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_provenance
;
np:hasPublicationInfo
dgn-np:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_assertion
a
np:Assertion
.
dgn-np:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_provenance
a
np:Provenance
.
dgn-np:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C2931822
a
ncit:C7057
.
dgn-gda:DGNa82b6d27d5236e7ea79b7ebf98859ac3
sio:SIO_000628
miriam-gene:2944
,
lld:C2931822
;
a
sio:SIO_001122
.
}
dgn-np:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_provenance
{
dgn-np:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_assertion
dcterms:description
"[The missense mutation in the coding region T1270533G of GSTM1 gene that causes an amino acid change does not affect the detoxification function of GSTM1, and the T1270533G polymorphism does not have apparent relations to NPC susceptibility in Chinese subjects in Guangdong Province.]. 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:19218107
;
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:NP74119.RAgsyfa9ymYTwBEzzzIvAfXkztOaoO1GGRtzSnASxy0hE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+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" .
}