@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac
> .
@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:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_head
{
this:
np:hasAssertion
dgn-np:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_assertion
;
np:hasProvenance
dgn-np:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_provenance
;
np:hasPublicationInfo
dgn-np:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_assertion
a
np:Assertion
.
dgn-np:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_provenance
a
np:Provenance
.
dgn-np:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN58063805d457cfd76736bcf97d6267f2
sio:SIO_000628
miriam-gene:5925
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_provenance
{
dgn-np:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_assertion
dcterms:description
"[Family history of breast cancer was found to be more common among patients with RB1 deletions and this trend was strengthened in cases where there were deletions at both the RB1 locus and on chromosome 17.]. 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:1746906
;
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:NP416032.RAuGY8NgOFXkogJhP58ArB1puZ_UuI_cAqhvTytUxv_Ac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:07+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" .
}