@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc
> .
@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:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_head
{
this:
np:hasAssertion
dgn-np:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_assertion
;
np:hasProvenance
dgn-np:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_provenance
;
np:hasPublicationInfo
dgn-np:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_assertion
a
np:Assertion
.
dgn-np:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_provenance
a
np:Provenance
.
dgn-np:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C0014175
a
ncit:C7057
.
dgn-gda:DGN4b2cab96ff108735cc83f6dac0796cb1
sio:SIO_000628
miriam-gene:1588
,
lld:C0014175
;
a
sio:SIO_001121
.
}
dgn-np:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_provenance
{
dgn-np:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_assertion
dcterms:description
"[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. 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:12620480
;
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:NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:40+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" .
}