@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390
> .
@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:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_head
{
this:
np:hasAssertion
dgn-np:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_assertion
;
np:hasProvenance
dgn-np:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_provenance
;
np:hasPublicationInfo
dgn-np:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_assertion
a
np:Assertion
.
dgn-np:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_provenance
a
np:Provenance
.
dgn-np:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_assertion
{
miriam-gene:51478
a
ncit:C16612
.
lld:C0014175
a
ncit:C7057
.
dgn-gda:DGN08676c0bdf9d1d6c43c509c87b56cbf1
sio:SIO_000628
miriam-gene:51478
,
lld:C0014175
;
a
sio:SIO_001121
.
}
dgn-np:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_provenance
{
dgn-np:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_assertion
dcterms:description
"[Additionally, endometriotic glandular cells are deficient in 17beta-hydroxysteroid dehydrogenase type 2, which converts E2 to estrone in the eutopic endometrium in response to P. Deficiency of this enzyme in endometriosis impairs the inactivation of E2 and may be a consequence of insensitivity to P.]. 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:10593363
;
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:NP270249.RAZCpfCDUL1P7XALpPGvYXNkj5GIlyl-NKeBqINFeB390130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}