@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto
> .
@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:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_head
{
this:
np:hasAssertion
dgn-np:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_assertion
;
np:hasProvenance
dgn-np:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_provenance
;
np:hasPublicationInfo
dgn-np:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_assertion
a
np:Assertion
.
dgn-np:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_provenance
a
np:Provenance
.
dgn-np:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C1704356
a
ncit:C7057
.
dgn-gda:DGN7f08597a6476609980f961150eeb3865
sio:SIO_000628
miriam-gene:675
,
lld:C1704356
;
a
sio:SIO_001121
.
}
dgn-np:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_provenance
{
dgn-np:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_assertion
dcterms:description
"[This trait is most probably not associated with mutations in the two major hereditary breast cancer genes since no cases of enchondroma or chondrosarcoma were found in Dutch BRCA1 and BRCA2 families.]. 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:14661035
;
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:NP439421.RA0CcgsGVE0ekhiRXvCWhj2D9UtP2RT0FWs62NeW77Wto130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}