@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU
> .
@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:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_head
{
this:
np:hasAssertion
dgn-np:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_assertion
;
np:hasProvenance
dgn-np:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_provenance
;
np:hasPublicationInfo
dgn-np:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_assertion
a
np:Assertion
.
dgn-np:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_provenance
a
np:Provenance
.
dgn-np:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNd78110d62a78b4a7e797aec641896402
sio:SIO_000628
miriam-gene:4360
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_provenance
{
dgn-np:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_assertion
dcterms:description
"[It has been controversial that men carrying a DNA mismatch repair (MMR) gene mutation (Lynch syndrome) are at heightened risk of prostate cancer given that an increased risk is likely to be modest and the prevalence of prostate cancer is high.]. 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:24425144
;
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:NP1145199.RAAQNuGaLLZxcYpaqQWVCH0VYxEZuC79GRxro1RCA5TXU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:25+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: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" .
}