@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc
> .
@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:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_head
{
this:
np:hasAssertion
dgn-np:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_assertion
;
np:hasProvenance
dgn-np:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_provenance
;
np:hasPublicationInfo
dgn-np:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_assertion
a
np:Assertion
.
dgn-np:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_provenance
a
np:Provenance
.
dgn-np:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_assertion
{
miriam-gene:5226
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN126622540403c9e551f4bdaf7a0224e4
sio:SIO_000628
miriam-gene:5226
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_provenance
{
dgn-np:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_assertion
dcterms:description
"[We further argue that a legal case for a duty to use PGD for medical benefit can be made in situations in which potential parents have chosen to conceive through in vitro fertilization and know that any children conceived are at substantial risk of having a serious genetic condition.]. 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:22452463
;
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:NP231230.RAg7fI-xnV0ntcwaq8lVN2SDNm1j9l569UOcFxc0a5iJc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:09+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" .
}