@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc
> .
@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:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_head
{
this:
np:hasAssertion
dgn-np:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_assertion
;
np:hasProvenance
dgn-np:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_provenance
;
np:hasPublicationInfo
dgn-np:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_assertion
a
np:Assertion
.
dgn-np:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_provenance
a
np:Provenance
.
dgn-np:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_assertion
{
miriam-gene:23274
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN0020eab44f07e19e58cef854e8b86438
sio:SIO_000628
miriam-gene:23274
,
lld:C0026769
;
a
sio:SIO_001122
.
}
dgn-np:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_provenance
{
dgn-np:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_assertion
dcterms:description
"[Although differences between individual families can only be suggested, the aggregate results in multiplex families demonstrate effect sizes that are increased as compared with those reported in previous studies for sporadic cases.]. 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:19506219
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP70866.RAqhQa2ZLaJcFYGY_iMgXMALnmVkSbECOamnaNnGnpqRc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:34+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" .
}