@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY
> .
@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:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_head
{
this:
np:hasAssertion
dgn-np:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_assertion
;
np:hasProvenance
dgn-np:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_provenance
;
np:hasPublicationInfo
dgn-np:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_assertion
a
np:Assertion
.
dgn-np:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_provenance
a
np:Provenance
.
dgn-np:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0032000
a
ncit:C7057
.
dgn-gda:DGN13d9a3d41f69728e47e980145ae5156a
sio:SIO_000628
miriam-gene:1565
,
lld:C0032000
;
a
sio:SIO_001121
.
}
dgn-np:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_provenance
{
dgn-np:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_assertion
dcterms:description
"[The data indicate the GSTM1 null and CYP2D6 EM genotypes are not associated with altered expression of p53 or, mutation of gsp and ras in these adenomas and, suggest the CYP2D6 PM genotype is associated with a reduced risk of pituitary adenomas and, that GSTM1*B confers greater protection than GSTM1*A.]. 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:7614700
;
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:NP895413.RA5EIDU-CN5k2CRoHafoms1Dddq88WO2vbtQQqvkfMgPY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:10+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" .
}