@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss
> .
@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:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_head
{
this:
np:hasAssertion
dgn-np:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_assertion
;
np:hasProvenance
dgn-np:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_provenance
;
np:hasPublicationInfo
dgn-np:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_assertion
a
np:Assertion
.
dgn-np:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_provenance
a
np:Provenance
.
dgn-np:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0346153
a
ncit:C7057
.
dgn-gda:DGN98e6a0746087e668d1d5c599ffc6faa0
sio:SIO_000628
miriam-gene:672
,
lld:C0346153
;
a
sio:SIO_001121
.
}
dgn-np:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_provenance
{
dgn-np:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_assertion
dcterms:description
"[Given that hereditary breast carcinoma is primarily due to germline mutations in one of two breast cancer susceptibility genes, BRCA1 and BRCA2, we have characterised the spectrum of BRCA mutations in a cohort of 37 individuals with early-onset disease (<or=40 years) and no reported family history.]. 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:18431501
;
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:NP667419.RAdhbYSLX34OULzQ5iHMOBfCmsP-k8SuFv47NqFoaItss130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:48+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" .
}