@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8
> .
@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:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_head
{
this:
np:hasAssertion
dgn-np:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_assertion
;
np:hasProvenance
dgn-np:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_provenance
;
np:hasPublicationInfo
dgn-np:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_assertion
a
np:Assertion
.
dgn-np:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_provenance
a
np:Provenance
.
dgn-np:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN26f7fc88e6ab4ac9ec1f3a9552dbd17f
sio:SIO_000628
miriam-gene:675
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_provenance
{
dgn-np:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_assertion
dcterms:description
"[It also asks why there should exist genetic variants associated with susceptibility to breast cancer other than mutations in BRCA1 and BRCA2, and what might be their modes of inheritance, allele frequencies and risks.]. 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:11305950
;
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:NP314642.RAuPCmG_DOMzhnEzI_P_GWXRl0cXalzXexz5VwTpBihE8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:08+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" .
}