@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg
> .
@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:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_head
{
this:
np:hasAssertion
dgn-np:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_assertion
;
np:hasProvenance
dgn-np:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_provenance
;
np:hasPublicationInfo
dgn-np:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_assertion
a
np:Assertion
.
dgn-np:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_provenance
a
np:Provenance
.
dgn-np:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0346153
a
ncit:C7057
.
dgn-gda:DGN7884d66412dfce7cedbce865e7e5ac74
sio:SIO_000628
miriam-gene:672
,
lld:C0346153
;
a
sio:SIO_001121
.
}
dgn-np:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_provenance
{
dgn-np:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_assertion
dcterms:description
"[The licence terms and business model proposed by Myriad Genetics Inc. for testing the hereditary breast cancer susceptibility genes BRCA1 and BRCA2 could stifle innovation (particularly if other companies adopt similar business models), and are likely to limit the ability to provide high quality public genetic testing services in Australia.]. 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:12914511
;
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:NP181218.RAM13ki-zvGrg8QJFb-sFaEnnzVtF5dZDPLiD5B976csg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}