@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A
> .
@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:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_head
{
this:
np:hasAssertion
dgn-np:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_assertion
;
np:hasProvenance
dgn-np:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_provenance
;
np:hasPublicationInfo
dgn-np:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_assertion
a
np:Assertion
.
dgn-np:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_provenance
a
np:Provenance
.
dgn-np:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_assertion
{
miriam-gene:5226
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGNf9c2cdcc0b450bf8f5097d72d2d2a91d
sio:SIO_000628
miriam-gene:5226
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_provenance
{
dgn-np:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_assertion
dcterms:description
"[Since the beginning of our PGD activity, we have had 43 PGD referrals for HD, of which 24 were from patients who know their genetic status and 19 from patients who do not wish to perform PT.]. 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:15470361
;
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:NP490982.RAYFiQn2qcq8jE2pGNQ-Td8FsURs4prYLS6uqMT6Vvm8A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}