@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo
> .
@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/v3.0.0/void/
> .
dgn-np:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_head
{
this:
np:hasAssertion
dgn-np:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_assertion
;
np:hasProvenance
dgn-np:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_provenance
;
np:hasPublicationInfo
dgn-np:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_assertion
a
np:Assertion
.
dgn-np:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_provenance
a
np:Provenance
.
dgn-np:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_assertion
{
miriam-gene:11200
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGNb56a607774414931454016f3a8d330d2
sio:SIO_000628
miriam-gene:11200
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_provenance
{
dgn-np:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_assertion
dcterms:description
"[These results suggest that testing for germline CHEK2 mutations improves the ability to predict the presence of prostate cancer in screened men, however, the clinical utility of incorporating DNA variants in the screening process is marginal.]. 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:23722471
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP862954.RAhsXUbucAu5MOxBp5FEMWnzF-tO5zSlNIy11eRk7JIeo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:24+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}