@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ
> .
@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:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_head
{
this:
np:hasAssertion
dgn-np:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_assertion
;
np:hasProvenance
dgn-np:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_assertion
a
np:Assertion
.
dgn-np:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_provenance
a
np:Provenance
.
dgn-np:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0346153
a
ncit:C7057
.
dgn-gda:DGNde891de444c213add88309768e2681e2
sio:SIO_000628
miriam-gene:675
,
lld:C0346153
;
a
sio:SIO_001121
.
}
dgn-np:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_provenance
{
dgn-np:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_assertion
dcterms:description
"[Numerous allelic variants identified in the familial breast cancer and DNA repair genes BRCA1 and BRCA2 are of unknown impact on protein function or clinical relevance, referred to as unclassified variants (UCV).]. 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:22729890
;
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:NP220573.RATKkeTWCibWOJ68apCDkuKqud0-eqXtvMfSPy-NqpgAQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}