@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE
> .
@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:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_head
{
this:
np:hasAssertion
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_assertion
;
np:hasProvenance
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_provenance
;
np:hasPublicationInfo
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_assertion
a
np:Assertion
.
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_provenance
a
np:Provenance
.
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_assertion
{
miriam-gene:5226
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN5f3a9ce3899b8c4b559449f2e8599e22
sio:SIO_000628
miriam-gene:5226
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_provenance
{
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_assertion
dcterms:description
"[Despite the numerous ethical objections and legal arguments, PGD for adult-onset cancers is today a reality and couples with an inherited predisposing mutation deserve the same respect, support and right to choose if their child will be born having an extremely high risk for cancer development as in the case of other life-threatening diseases for which prenatal screening has become a standard.]. 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:19785065
;
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:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:22+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" .
}