@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4
> .
@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:NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4130_head
{
this:
np:hasAssertion
dgn-np:NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4130_assertion
a
np:Assertion
.
dgn-np:NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4130_provenance
a
np:Provenance
.
dgn-np:NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0032000
a
ncit:C7057
.
dgn-gda:DGNb84db5cccf596bd6069e238d6da64ba0
sio:SIO_000628
miriam-gene:7157
,
lld:C0032000
;
a
sio:SIO_001121
.
}
dgn-np:NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4130_provenance
{
dgn-np:NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4130_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:NP720474.RALYCnLE8GRySgY4fm3hRnRMVJtMcMihMNBFuETpglid4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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
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"v2.1.0" .
}