@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_head
{
this:
np:hasAssertion
dgn-np:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_assertion
;
np:hasProvenance
dgn-np:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_provenance
;
np:hasPublicationInfo
dgn-np:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_assertion
a
np:Assertion
.
dgn-np:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_provenance
a
np:Provenance
.
dgn-np:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0014175
a
ncit:C7057
.
dgn-gda:DGNfef1f2486a1bf2f119db4978177a8a02
sio:SIO_000628
miriam-gene:2944
,
lld:C0014175
;
a
sio:SIO_001121
.
}
dgn-np:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_provenance
{
dgn-np:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_assertion
dcterms:description
"[The combination of CYP1A1 m1 polymorphism and GSTM1 null deletion is closely associated with penetration of the endometriosis phenotype, whereas GSTT1 null deletion may add to the penetration of this trait.]. 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:11730751
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP337919.RAwE2Sr7yRkjPvTaHAaYB_w9m0zDqOCJrSrrCmgLVyQEg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:18+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}