@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4
> .
@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:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_head
{
this:
np:hasAssertion
dgn-np:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_assertion
;
np:hasProvenance
dgn-np:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_provenance
;
np:hasPublicationInfo
dgn-np:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_assertion
a
np:Assertion
.
dgn-np:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_provenance
a
np:Provenance
.
dgn-np:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_assertion
{
miriam-gene:11200
a
ncit:C16612
.
lld:C0346153
a
ncit:C7057
.
dgn-gda:DGN706551c993f173fb7fe12da47dc7a83a
sio:SIO_000628
miriam-gene:11200
,
lld:C0346153
;
a
sio:SIO_001121
.
}
dgn-np:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_provenance
{
dgn-np:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_assertion
dcterms:description
"[To establish the importance of CHEK2 mutations for familial breast cancer incidence in the German population, we have screened all 14 of the coding exons in 516 families negative for mutations in both the BRCA1 and BRCA2 genes.]. 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:15095295
;
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:NP346441.RAss_khs1Cmk0-imUIYo6Nb5Io5PbO9lrsZ2gk1R9z4J4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:23+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" .
}