@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao
> .
@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:NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao130_head
{
this:
np:hasAssertion
dgn-np:NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao130_assertion
a
np:Assertion
.
dgn-np:NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao130_provenance
a
np:Provenance
.
dgn-np:NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNdf10367e7498de5791ac38bbed5d6b54
sio:SIO_000628
miriam-gene:675
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao130_provenance
{
dgn-np:NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao130_assertion
dcterms:description
"[To detect potential novel gene defects that may contribute to hereditary BC susceptibility, 143 patients belonging to 143 Chilean families tested for BRCA1 and BRCA2 mutations were screened for mutations in RAD51, using conformational sensitive gel electrophoresis (CSGE) and DNA sequencing.]. 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:17889711
;
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:NP631364.RAlppHnx38GNap-om640M3iwNk1sfEzmaeGOBfXjKqqao130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:31+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
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;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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" .
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pav:version
"v4.0.0" .
}