@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA
> .
@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:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_head
{
this:
np:hasAssertion
dgn-np:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_assertion
;
np:hasProvenance
dgn-np:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_provenance
;
np:hasPublicationInfo
dgn-np:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_assertion
a
np:Assertion
.
dgn-np:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_provenance
a
np:Provenance
.
dgn-np:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C0014175
a
ncit:C7057
.
dgn-gda:DGN0bad5b91efd289232d8a4dd4dde9d382
sio:SIO_000628
miriam-gene:133482
,
lld:C0014175
;
a
sio:SIO_001121
.
}
dgn-np:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_provenance
{
dgn-np:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_assertion
dcterms:description
"[The null genetic polymorphism in the gene encoding the GST class mu (GSTM1) enzyme has been reported to be significantly elevated in endometriosis patients and may represent an endometriosis susceptibility allele.]. 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:11159742
;
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:NP820864.RA_MtIDpDIBi3ehJE3lknKaaEOPk5kJ0JGxJznJYz_veA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}