@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA
> .
@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:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_head
{
this:
np:hasAssertion
dgn-np:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_assertion
;
np:hasProvenance
dgn-np:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_provenance
;
np:hasPublicationInfo
dgn-np:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_assertion
a
np:Assertion
.
dgn-np:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_provenance
a
np:Provenance
.
dgn-np:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGNa663921c1cce3f7917be4ad9b7d01e7a
sio:SIO_000628
miriam-gene:2952
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_provenance
{
dgn-np:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_assertion
dcterms:description
"[The associations of polymorphisms of other metabolizing enzymes (CYP1A1, GSTM1 and GSTT1) with the MM risk were investigated in 116 Korean MM patients and 176 Korean controls using TaqMan allelic discrimination and multiplex polymerase chain reaction.]. 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:18285692
;
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:NP911919.RAIR4St7-c0QIjrhDRYgL8fbQYvU-imJUlKbrMIpoqMOA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}