@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno
> .
@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:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_head
{
this:
np:hasAssertion
dgn-np:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_assertion
;
np:hasProvenance
dgn-np:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_provenance
;
np:hasPublicationInfo
dgn-np:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_assertion
a
np:Assertion
.
dgn-np:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_provenance
a
np:Provenance
.
dgn-np:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C1512981
a
ncit:C7057
.
dgn-gda:DGN066d9c7a1140a7e856d3f830444c6312
sio:SIO_000628
miriam-gene:675
,
lld:C1512981
;
a
sio:SIO_001121
.
}
dgn-np:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_provenance
{
dgn-np:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_assertion
dcterms:description
"[Our results, indicating that missense mutations of BRCA1 and BRCA2 tend to predominate over frameshifts or nonsense mutations in Japanese breast cancer families, will contribute significantly to an understanding of mammary tumorigenesis in Japan, and will be of vital importance for future genetic testing.]. 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:9609997
;
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:NP813956.RA80VYtcM6FXnYS2xe0MlRlBcIhluPIY8sLQp4tePdzno130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:19+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" .
}