@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_head
{
this:
np:hasAssertion
dgn-np:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_assertion
;
np:hasProvenance
dgn-np:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_assertion
a
np:Assertion
.
dgn-np:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_provenance
a
np:Provenance
.
dgn-np:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_assertion
{
miriam-gene:9560
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN50422da741f1642d17eb54a116915344
sio:SIO_000628
miriam-gene:9560
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_provenance
{
dgn-np:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_assertion
dcterms:description
"[Novel therapeutic interventions for Down syndrome and the monogenic and polygenic disorders that map to HC21 will be designed and tried based on the knowledge of the disease pathogenesis resulting from the genomic analysis.]. 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:9693027
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1401127.RAJlSvifZS3M-npPsWWXZf4pKm3WU5EETY6E-BMnVNFJo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:21+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}