@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A
> .
@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:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_head
{
this:
np:hasAssertion
dgn-np:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_assertion
;
np:hasProvenance
dgn-np:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_provenance
;
np:hasPublicationInfo
dgn-np:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_assertion
a
np:Assertion
.
dgn-np:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_provenance
a
np:Provenance
.
dgn-np:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_assertion
{
miriam-gene:2973
a
ncit:C16612
.
lld:C0040517
a
ncit:C7057
.
dgn-gda:DGN859a28ef9752c82ad32c3e43d7a3a56a
sio:SIO_000628
miriam-gene:2973
,
lld:C0040517
;
a
sio:SIO_001121
.
}
dgn-np:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_provenance
{
dgn-np:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_assertion
dcterms:description
"[Propelled by the gradual availability of large scale TS cohorts, and novel methodologies for the study of both common and rare genetic variants, the new era of TS genetics holds the promise to identify novel targets for improved therapies.]. 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:23333760
;
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:NP901571.RA5SlK4IBqsiRm8s4Xqt346r21Jw-fWt319iIJz9HO39A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:14+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" .
}