@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q
> .
@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:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_head
{
this:
np:hasAssertion
dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_assertion
;
np:hasProvenance
dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_assertion
a
np:Assertion
.
dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_provenance
a
np:Provenance
.
dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_assertion
{
miriam-gene:8289
a
ncit:C16612
.
lld:C0014175
a
ncit:C7057
.
dgn-gda:DGNe727f069ac0faf78a9c5303fb09879ec
sio:SIO_000628
miriam-gene:8289
,
lld:C0014175
;
a
sio:SIO_001121
.
}
dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_provenance
{
dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_assertion
dcterms:description
"[Endometriosis is characterized by genetic instability: like neoplasms endometriosis seems to be monoclonal in origin, several studies have documented loss of heterozygosity (LOH) in endometriosis, data suggest that mutation of the tumor suppressor gene PTEN play a part in the malignant transformation of endometriosis, some studies have revealed TP53 mutations in endometriotic lesions, and mutation of ARID1A seems to be an important early event in the malignant transformation of endometriosis to endometrioid and clear cell carcinomas.]. 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:22032835
;
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:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:11+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" .
}