@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ
> .
@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:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_head
{
this:
np:hasAssertion
dgn-np:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_assertion
;
np:hasProvenance
dgn-np:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_assertion
a
np:Assertion
.
dgn-np:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_provenance
a
np:Provenance
.
dgn-np:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGNc81bf556b0629ddd07e05139360a4a4f
sio:SIO_000628
miriam-gene:675
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_provenance
{
dgn-np:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_assertion
dcterms:description
"[The NLSs locate between the germline mutation found in the most downstream position and the polymorphic stop codon, suggesting that defects in the proper nuclear transport of the BRCA2 protein are causative of carcinogenesis.]. 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:10733923
;
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:NP279013.RA5S68srMpvUdwLedqI8wgkW5gHXkb6Y7XE2I2yDVD6dQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:52+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}