@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1154066.RArZK6DLXw9zzNfkpqpr5P6RnyIABVtr4AGPIMG2oxKUs
> .
@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:NP1154066.RArZK6DLXw9zzNfkpqpr5P6RnyIABVtr4AGPIMG2oxKUs130_head
{
this:
np:hasAssertion
dgn-np:NP1154066.RArZK6DLXw9zzNfkpqpr5P6RnyIABVtr4AGPIMG2oxKUs130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1154066.RArZK6DLXw9zzNfkpqpr5P6RnyIABVtr4AGPIMG2oxKUs130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP1154066.RArZK6DLXw9zzNfkpqpr5P6RnyIABVtr4AGPIMG2oxKUs130_assertion
a
np:Assertion
.
dgn-np:NP1154066.RArZK6DLXw9zzNfkpqpr5P6RnyIABVtr4AGPIMG2oxKUs130_provenance
a
np:Provenance
.
dgn-np:NP1154066.RArZK6DLXw9zzNfkpqpr5P6RnyIABVtr4AGPIMG2oxKUs130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:56606
a
ncit:C16612
.
lld:C0008925
a
ncit:C7057
.
dgn-gda:DGNc3fe039f9bfae13bcf46562227cdeaf0
sio:SIO_000628
miriam-gene:56606
,
lld:C0008925
;
a
sio:SIO_001121
.
}
dgn-np:NP1154066.RArZK6DLXw9zzNfkpqpr5P6RnyIABVtr4AGPIMG2oxKUs130_provenance
{
dgn-np:NP1154066.RArZK6DLXw9zzNfkpqpr5P6RnyIABVtr4AGPIMG2oxKUs130_assertion
dcterms:description
"[Although further replication studies are critical to confirming these findings, these results illustrate how genetic associations for nonsyndromic CP can be missed if potential GxE interaction is not taken into account, and this study suggest SLC2A9 and WDR1 should be considered as candidate genes for CP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:24516586
;
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:NP1154066.RArZK6DLXw9zzNfkpqpr5P6RnyIABVtr4AGPIMG2oxKUs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:29+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
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;
pav:authoredBy
<
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> , <
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
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pav:version
"v4.0.0" .
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