@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo
> .
@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:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_head
{
this:
np:hasAssertion
dgn-np:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_assertion
;
np:hasProvenance
dgn-np:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_provenance
;
np:hasPublicationInfo
dgn-np:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_assertion
a
np:Assertion
.
dgn-np:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_provenance
a
np:Provenance
.
dgn-np:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_assertion
{
miriam-gene:26227
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN5c1b2ce530bfcd314d24b5abc8e1e8e4
sio:SIO_000628
miriam-gene:26227
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_provenance
{
dgn-np:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_assertion
dcterms:description
"[Factors playing a role in the decision-making process were the carrier's sex, ethical issues about PD and PGD, the strength of the desire to have children, illness representations including personal experiences with HD in the family and the technological imperative.]. 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:17245406
;
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:NP768526.RADItqpe2uRQWMPs8yuY0lH2hIUlqPqutaD1eSXNvfVKo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}