@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0
> .
@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:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_head
{
this:
np:hasAssertion
dgn-np:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_assertion
;
np:hasProvenance
dgn-np:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_provenance
;
np:hasPublicationInfo
dgn-np:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_assertion
a
np:Assertion
.
dgn-np:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_provenance
a
np:Provenance
.
dgn-np:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0029463
a
ncit:C7057
.
dgn-gda:DGN89a907f575dce6718650132efd44de84
sio:SIO_000628
miriam-gene:675
,
lld:C0029463
;
a
sio:SIO_001121
.
}
dgn-np:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_provenance
{
dgn-np:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_assertion
dcterms:description
"[The increased risk of ovarian cancer is consistent with germline mutations in the BRCA1 and BRCA2 genes, while the risk of soft tissue and bone sarcomas may reflect the association of these tumours with Li-Fraumeni syndrome.]. 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:10962444
;
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:NP877796.RAX7JiyozTUE1alBlkUYBz7VvpzansaZxwdc9mH88uoc0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+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" .
}