@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw
> .
@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:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_head
{
this:
np:hasAssertion
dgn-np:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_assertion
;
np:hasProvenance
dgn-np:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_provenance
;
np:hasPublicationInfo
dgn-np:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_assertion
a
np:Assertion
.
dgn-np:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_provenance
a
np:Provenance
.
dgn-np:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGNfcad42ec5feb10694bd7197d24b8f21f
sio:SIO_000628
miriam-gene:472
,
lld:C1458155
;
a
sio:SIO_001121
.
}
dgn-np:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_provenance
{
dgn-np:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_assertion
dcterms:description
"[The fact that women carriers of ATM mutations can have an increased risk of developing breast cancer and that many sporadic breast tumours have reduced levels of the ATM protein broadens the scope of ATM's tumour suppressor within the breast.]. 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:12196249
;
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:NP439834.RADBtoUBea-_UotD67rN8cPn63_XhAGh1W3U07EKMiNjw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}