@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E
> .
@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:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_head
{
this:
np:hasAssertion
dgn-np:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_assertion
;
np:hasProvenance
dgn-np:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_provenance
;
np:hasPublicationInfo
dgn-np:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_assertion
a
np:Assertion
.
dgn-np:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_provenance
a
np:Provenance
.
dgn-np:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN88ae548627c5c25790bcd3f7dd26d0ff
sio:SIO_000628
miriam-gene:675
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_provenance
{
dgn-np:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_assertion
dcterms:description
"[BRCA1 and BRCA2 mutation carriers could potentially be among the first groups of individuals for whom clinically applicable risk profiling could be developed using the common breast cancer susceptibility variants identified through GWAS.]. 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:21285145
;
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:NP869423.RALeiRtYrGdVMgXzE3FaDyyW9mXlZzhsgcogdx2XALR_E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:18+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" .
}