@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w
> .
@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:NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w130_head
{
this:
np:hasAssertion
dgn-np:NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w130_assertion
a
np:Assertion
.
dgn-np:NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w130_provenance
a
np:Provenance
.
dgn-np:NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w130_assertion
{
miriam-gene:4072
a
ncit:C16612
.
lld:C1883486
a
ncit:C7057
.
dgn-gda:DGN22251abfc91f00b47c9e05340a88966c
sio:SIO_000628
miriam-gene:4072
,
lld:C1883486
;
a
sio:SIO_001121
.
}
dgn-np:NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w130_provenance
{
dgn-np:NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w130_assertion
dcterms:description
"[The risk of endometrial cancer in the entire group of EPCAM deletion carriers is significantly lower than that in MSH2 mutation carriers, but the actual risk appears to be dependent on the size and location of the EPCAM deletion.]. 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:23264089
;
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:NP1038337.RAorJ9d1s82G78o_O9xx8wDsbpywCxp0mpLq9GlkHzw3w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:36+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
<
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> , <
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" .
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pav:version
"v4.0.0" .
}