@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8
> .
@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:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_head
{
this:
np:hasAssertion
dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_assertion
;
np:hasProvenance
dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_provenance
;
np:hasPublicationInfo
dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_assertion
a
np:Assertion
.
dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_provenance
a
np:Provenance
.
dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_assertion
{
miriam-gene:11200
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN787b77819d61430ec6b8c0f896ad8cb0
sio:SIO_000628
miriam-gene:11200
,
lld:C0596263
;
a
sio:SIO_001122
.
}
dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_provenance
{
dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_assertion
dcterms:description
"[This study provides further evidence that sequence variation in CHEK2 is associated with an increased risk of breast cancer, and implies that tumorigenesis in association with CHEK2 mutations does not involve loss of the wild type allele.]. 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:12454775
;
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:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:35+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" .
}