@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M
> .
@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:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_head
{
this:
np:hasAssertion
dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_assertion
;
np:hasProvenance
dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_provenance
;
np:hasPublicationInfo
dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_assertion
a
np:Assertion
.
dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_provenance
a
np:Provenance
.
dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0018553
a
ncit:C7057
.
dgn-gda:DGN262851a1cda08558f090651f3a5dbe9c
sio:SIO_000628
miriam-gene:675
,
lld:C0018553
;
a
sio:SIO_001121
.
}
dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_provenance
{
dgn-np:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_assertion
dcterms:description
"[Whilst breast cancer occurring in patients in Li-Fraumeni and Cowden's syndrome families is of great importance, the more frequent scenario is that of women, or indeed of men, presenting with breast cancer with an underlying germline mutation in BRCA1 or BRCA2.]. 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:19027287
;
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:NP897687.RAowwkMHTvAlyzCS1LBrzUuYy4gnDJeFbSKhmW4RFK_-M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:12+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" .
}