@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA
> .
@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:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_head
{
this:
np:hasAssertion
dgn-np:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_assertion
;
np:hasProvenance
dgn-np:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_provenance
;
np:hasPublicationInfo
dgn-np:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_assertion
a
np:Assertion
.
dgn-np:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_provenance
a
np:Provenance
.
dgn-np:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN5234b95d79a40efe60f8cc0bb7fd37bb
sio:SIO_000628
miriam-gene:675
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_provenance
{
dgn-np:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_assertion
dcterms:description
"[This approach has identified two genetic variants that are associated with colorectal cancer risk in Lynch Syndrome, and five polymorphisms that are associated with the risk of breast cancer for BRCA1 and/or BRCA2 mutation carriers.]. 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:20399636
;
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:NP760764.RAACCXnr6rUwzUYHHS7_rEYO4W4Fv0tediEq7fxszjZYA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}