@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE
> .
@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:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_head
{
this:
np:hasAssertion
dgn-np:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_assertion
;
np:hasProvenance
dgn-np:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_provenance
;
np:hasPublicationInfo
dgn-np:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_assertion
a
np:Assertion
.
dgn-np:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_provenance
a
np:Provenance
.
dgn-np:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_assertion
{
miriam-gene:1240
a
ncit:C16612
.
lld:C1867981
a
ncit:C7057
.
dgn-gda:DGNe1854f83f3ccf0de757a51a085899289
sio:SIO_000628
miriam-gene:1240
,
lld:C1867981
;
a
sio:SIO_001121
.
}
dgn-np:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_provenance
{
dgn-np:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_assertion
dcterms:description
"[DNA sequencing of the coding exons of six candidate genes (CRY1, PWP1, ASCL4, PRDM4, KIAA0789 and CMKLR1) on the basis of their location in the critical overlap interval, failed to detect any mutation in DSAP patients.]. 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:16078733
;
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:NP376442.RAcAUl0_lIm1WmgwMf9WzAQU4Wvq16HXOLckXl5SxHhlE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}