@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4
> .
@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:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_head
{
this:
np:hasAssertion
dgn-np:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_assertion
;
np:hasProvenance
dgn-np:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_provenance
;
np:hasPublicationInfo
dgn-np:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_assertion
a
np:Assertion
.
dgn-np:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_provenance
a
np:Provenance
.
dgn-np:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1261473
a
ncit:C7057
.
dgn-gda:DGN8668263d93521ffd37a878e296eeb98d
sio:SIO_000628
miriam-gene:672
,
lld:C1261473
;
a
sio:SIO_001121
.
}
dgn-np:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_provenance
{
dgn-np:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_assertion
dcterms:description
"[In this study, 23 unrelated individuals from families with one case of sarcoma and at least one case of breast cancer were screened for mutations in the TP53, BRCA1 and BRCA2 genes.]. 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:17224268
;
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:NP654563.RA4LkfvcSGL1Kn91KJlWTmqMONkFuW7UfshskruXNlQR4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:34+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" .
}