@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s
> .
@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:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_head
{
this:
np:hasAssertion
dgn-np:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_assertion
;
np:hasProvenance
dgn-np:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_provenance
;
np:hasPublicationInfo
dgn-np:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_assertion
a
np:Assertion
.
dgn-np:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_provenance
a
np:Provenance
.
dgn-np:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0007103
a
ncit:C7057
.
dgn-gda:DGN0fbbe739731d97818883cc8e1e5a11bf
sio:SIO_000628
miriam-gene:4436
,
lld:C0007103
;
a
sio:SIO_001122
.
}
dgn-np:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_provenance
{
dgn-np:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_assertion
dcterms:description
"[Unselected Jewish women with EC who were diagnosed from January 1982 to January 2008 were genotyped for the predominant mutations in Jewish individuals in BRCA1 (185delAG, 5382InsC, Tyr978X) BRCA2 (6174delT), MSH2 (A636P, 324delCA) and MSH6 (c.3984_3987dup).]. 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:20850175
;
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:NP839982.RAMvjq0PCFHpBZF2qDr6V8Nf-1hta9DuyP9RatKlp9j3s130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:05+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" .
}