@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo
> .
@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:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_head
{
this:
np:hasAssertion
dgn-np:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_assertion
;
np:hasProvenance
dgn-np:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_provenance
;
np:hasPublicationInfo
dgn-np:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_assertion
a
np:Assertion
.
dgn-np:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_provenance
a
np:Provenance
.
dgn-np:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0346153
a
ncit:C7057
.
dgn-gda:DGNe09e9cd662f4a15b9b9d19bbbe204204
sio:SIO_000628
miriam-gene:472
,
lld:C0346153
;
a
sio:SIO_001121
.
}
dgn-np:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_provenance
{
dgn-np:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_assertion
dcterms:description
"[We postulate that our discrepancies with other reports related to the associated ATM alleles to hereditary breast cancer, as well as discrepancies in the literature between other groups, could be explained by the diversity in the ethnic origins of families gathered in a sole study, and the selection of the control group.]. 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:17351744
;
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:NP233742.RAOqyOIf-SDbdMLkPZQc70cKErVkdVJ8ZCgQ02HGrkdZo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:11+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" .
}