@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU
> .
@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:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_head
{
this:
np:hasAssertion
dgn-np:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_assertion
;
np:hasProvenance
dgn-np:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_provenance
;
np:hasPublicationInfo
dgn-np:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_assertion
a
np:Assertion
.
dgn-np:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_provenance
a
np:Provenance
.
dgn-np:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C2931038
a
ncit:C7057
.
dgn-gda:DGN31e7673b8366f96ae7dbb9453a50d8c4
sio:SIO_000628
miriam-gene:675
,
lld:C2931038
;
a
sio:SIO_001121
.
}
dgn-np:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_provenance
{
dgn-np:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_assertion
dcterms:description
"[As the prevalence of those mutations in the setting of familial pancreatic cancer is still not well defined for the German population, we evaluated the presence of BRCA2 and CDKN2a germline mutations in a large cohort of familial pancreatic cancer (FPC) families from the German National Case Collection for Familial Pancreatic Cancer (FaPaCa).]. 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:20195775
;
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:NP648248.RADIyVamy6N4hO7ADgmXT6vcL4hxNQxFrWJGWmIm_geaU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}