@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194
> .
@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:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_head
{
this:
np:hasAssertion
dgn-np:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_assertion
;
np:hasProvenance
dgn-np:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_provenance
;
np:hasPublicationInfo
dgn-np:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_assertion
a
np:Assertion
.
dgn-np:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_provenance
a
np:Provenance
.
dgn-np:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_assertion
{
miriam-gene:4683
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN7928f66be1e59bb387113da047f65733
sio:SIO_000628
miriam-gene:4683
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_provenance
{
dgn-np:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_assertion
dcterms:description
"[Individuals who are heterozygous for NBN mutations are clinically asymptomatic, but may display an elevated risk for certain cancers including, but not limited to, ovarian and prostate cancer as well as various lymphoid malignancies.]. 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:22864661
;
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:NP521372.RAw10_RkpQl7hmQYS94dpJHBodFi6YlN7mI2jk0Ih0194130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}