@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M
> .
@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:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_head
{
this:
np:hasAssertion
dgn-np:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_assertion
;
np:hasProvenance
dgn-np:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance
;
np:hasPublicationInfo
dgn-np:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_assertion
a
np:Assertion
.
dgn-np:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance
a
np:Provenance
.
dgn-np:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_assertion
{
miriam-gene:10498
a
ncit:C16612
.
lld:C0080178
a
ncit:C7057
.
dgn-gda:DGNc681d764cb0b01d1a46d6a261373d88e
sio:SIO_000628
miriam-gene:10498
,
lld:C0080178
;
a
sio:SIO_001122
.
}
dgn-np:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_provenance
{
dgn-np:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_assertion
dcterms:description
"[Modest associations were observed in CITED2, EP300, CREBBP, TFAP2A and CARM1 but not ALX1. However, these modest associations were not statistically significant after correction for multiple comparisons. Searching for potential functional variants and rare causal mutations is warranted in these genes.]. 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:20932315
;
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:NP89238.RAoC-0_INHUx6qIXMXh-f5DQTaNY0y5DZ0v9TrITUUq8M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:44+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" .
}