@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI
> .
@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:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_head
{
this:
np:hasAssertion
dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_assertion
;
np:hasProvenance
dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_provenance
;
np:hasPublicationInfo
dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_assertion
a
np:Assertion
.
dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_provenance
a
np:Provenance
.
dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGN635846fff4b6edfc219f3505e50ae1a1
sio:SIO_000628
miriam-gene:675
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_provenance
{
dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_assertion
dcterms:description
"[For gynecologists, knowledge of cancer susceptibility genes such as BRCA1 and BRCA2 and the genetic syndrome hereditary nonpolyposis colorectal cancer (Lynch syndrome II) affects how patients are screened for ovarian and endometrial cancers.]. 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:16582132
;
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:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
}