@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg
> .
@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:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_head
{
this:
np:hasAssertion
dgn-np:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_assertion
;
np:hasProvenance
dgn-np:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_provenance
;
np:hasPublicationInfo
dgn-np:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_assertion
a
np:Assertion
.
dgn-np:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_provenance
a
np:Provenance
.
dgn-np:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_assertion
{
miriam-gene:6785
a
ncit:C16612
.
lld:C1838644
a
ncit:C7057
.
dgn-gda:DGN1aadcd30967cdd483e08f0c8a40f2bfa
sio:SIO_000628
miriam-gene:6785
,
lld:C1838644
;
a
sio:SIO_001121
.
}
dgn-np:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_provenance
{
dgn-np:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_assertion
dcterms:description
"[To explore whether the STGD3-like phenotype in the kindred is linked to ELOVL4 gene or associated with any other identified STGD gene, we extracted genomic DNA from leukocytes of peripheral blood from the available family members and 50 normal controls for mutation analysis.]. 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:16364203
;
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:NP756211.RALESWFjAXSvGiXWzeclau9DWoZd6-bTcy3y4yM274xhg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:38+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" .
}