@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU
> .
@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:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_head
{
this:
np:hasAssertion
dgn-np:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_assertion
;
np:hasProvenance
dgn-np:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_provenance
;
np:hasPublicationInfo
dgn-np:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_assertion
a
np:Assertion
.
dgn-np:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_provenance
a
np:Provenance
.
dgn-np:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_assertion
{
miriam-gene:4830
a
ncit:C16612
.
lld:C1303073
a
ncit:C7057
.
dgn-gda:DGNa821f3c3c2cbc35909d09d4998fcd325
sio:SIO_000628
miriam-gene:4830
,
lld:C1303073
;
a
sio:SIO_001121
.
}
dgn-np:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_provenance
{
dgn-np:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_assertion
dcterms:description
"[Evidence on the effects of disclosing carrier results identified through newborn screening (NBS) is needed to develop effective strategies for managing these results, and to inform debate about contradictory policies governing genetic testing in minors in the context of NBS relative to clinical care.]. 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:18956236
;
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:NP632174.RAFb8gRSwsLw9-znnAmsvFC1s4V_eSbPoHen_PkycfAMU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:21+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" .
}