@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE
> .
@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:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_head
{
this:
np:hasAssertion
dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_assertion
;
np:hasProvenance
dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_provenance
;
np:hasPublicationInfo
dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_assertion
a
np:Assertion
.
dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_provenance
a
np:Provenance
.
dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN7fb45fff2b8bd9b23f863a1f72a47840
sio:SIO_000628
miriam-gene:672
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_provenance
{
dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_assertion
dcterms:description
"[In 15 of these 22 cases, the relevant history suggestive of hereditary breast cancer and OC (due to BRCA1 or BRCA2 mutations) or Lynch syndrome had been documented, but no action was recorded, and its significance was not appreciated.]. 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:22274317
;
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:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:58+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" .
}