@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI
> .
@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:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_head
{
this:
np:hasAssertion
dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_assertion
;
np:hasProvenance
dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_provenance
;
np:hasPublicationInfo
dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_assertion
a
np:Assertion
.
dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_provenance
a
np:Provenance
.
dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_assertion
{
miriam-gene:4683
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN5c9012879092c58fcedb2b9d3f3e6873
sio:SIO_000628
miriam-gene:4683
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_provenance
{
dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_assertion
dcterms:description
"[These findings suggest that heterozygous carriers of the NBS1 founder mutation exhibit increased susceptibility to prostate cancer and that the cancers that develop in the prostates of carriers are functionally homozygous for the mutation.]. 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:14973119
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}