@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA
> .
@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:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_head
{
this:
np:hasAssertion
dgn-np:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_assertion
;
np:hasProvenance
dgn-np:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_provenance
;
np:hasPublicationInfo
dgn-np:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_assertion
a
np:Assertion
.
dgn-np:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_provenance
a
np:Provenance
.
dgn-np:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0014175
a
ncit:C7057
.
dgn-gda:DGN7eaaf8d15c0f58139e949f8d85931776
sio:SIO_000628
miriam-gene:7248
,
lld:C0014175
;
a
sio:SIO_001121
.
}
dgn-np:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_provenance
{
dgn-np:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_assertion
dcterms:description
"[Our own studies have shown that genetic alterations, as shown by loss of heterozygosity, are relatively common in endometriosis implying that tumour suppressor gene inactivation is likely to be involved in the proliferation and maintenance of all endometriotic implants.]. 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:11212068
;
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:NP308737.RAotHKmyg47SAtLNhdIbtykJ5DlBTII6_ohgD59T78nTA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:05+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" .
}