@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE
> .
@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/v3.0.0/void/
> .
dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_head
{
this:
np:hasAssertion
dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_assertion
;
np:hasProvenance
dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_provenance
;
np:hasPublicationInfo
dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_assertion
a
np:Assertion
.
dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_provenance
a
np:Provenance
.
dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_assertion
{
miriam-gene:115761
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN0b8e9ab2c7d01215bc69c04d4c312a84
sio:SIO_000628
miriam-gene:115761
,
lld:C0006826
;
a
sio:SIO_001122
.
}
dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_provenance
{
dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_assertion
dcterms:description
"[The ARLTS1 mutation Trp149Stop and Cys148Arg have been shown to be associated with familial cancers, but limited information is available regarding the impact of ARLTS1 variants on familial ovarian cancer (OC).]. 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:19509554
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:30+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}