@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc
> .
@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:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_head
{
this:
np:hasAssertion
dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_assertion
;
np:hasProvenance
dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_provenance
;
np:hasPublicationInfo
dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_assertion
a
np:Assertion
.
dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_provenance
a
np:Provenance
.
dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNae64f9d5b0aace0e18b9cf9ca41f0652
sio:SIO_000628
miriam-gene:672
,
lld:C0006826
;
a
sio:SIO_001122
.
}
dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_provenance
{
dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_assertion
dcterms:description
"[The especially frequent carrier state among the Ashkenazi Jewish population coupled with the high prevalence of BRCA1 and BRCA2 in the same population has led us to search for coinheritance affecting the potential for cancer development.]. 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:15726604
;
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:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}