@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ
> .
@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:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_head
{
this:
np:hasAssertion
dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_assertion
;
np:hasProvenance
dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_assertion
a
np:Assertion
.
dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_provenance
a
np:Provenance
.
dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_assertion
{
miriam-gene:24
a
ncit:C16612
.
lld:C0015397
a
ncit:C7057
.
dgn-gda:DGN368e47b7b1bb626b5b3955612120e99a
sio:SIO_000628
miriam-gene:24
,
lld:C0015397
;
a
sio:SIO_001121
.
}
dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_provenance
{
dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_assertion
dcterms:description
"[Screening of increasingly large numbers of patients would help to determine whether this can be explained by ethnic differences, or is an indicator of extensive allelic heterogeneity of ABCR in STGD1 and other eye diseases.]. 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:10711710
;
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:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}