@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY
> .
@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:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_head
{
this:
np:hasAssertion
dgn-np:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_assertion
;
np:hasProvenance
dgn-np:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance
;
np:hasPublicationInfo
dgn-np:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_assertion
a
np:Assertion
.
dgn-np:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance
a
np:Provenance
.
dgn-np:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGNc00ad073a1a1e1a2ef6c5da912a4d2b6
sio:SIO_000628
miriam-gene:672
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance
{
dgn-np:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_assertion
dcterms:description
"[The aim of this study was to characterize eight of the most common reported missense mutations in BRCA1 and BRCA2 occurring in patients tested for hereditary risk of breast and ovarian cancers.]. 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:12215251
;
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:NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:31+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" .
}