@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM
> .
@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:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_head
{
this:
np:hasAssertion
dgn-np:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_assertion
;
np:hasProvenance
dgn-np:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_provenance
;
np:hasPublicationInfo
dgn-np:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_assertion
a
np:Assertion
.
dgn-np:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_provenance
a
np:Provenance
.
dgn-np:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_assertion
{
miriam-gene:4167
a
ncit:C16612
.
lld:C0730294
a
ncit:C7057
.
dgn-gda:DGN7baf7eab468b3633b22d3fec73a7f101
sio:SIO_000628
miriam-gene:4167
,
lld:C0730294
;
a
sio:SIO_001121
.
}
dgn-np:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_provenance
{
dgn-np:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_assertion
dcterms:description
"[To study the North Carolina macular dystrophy phenotype (MCDR1) in multiple families of different ethnic backgrounds, to determine the genetic relationships of these families, and to determine the minimal candidate region of the MCDR1 gene.]. 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:10360311
;
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:NP848801.RAKTvikt_zv3jsAPpSIciMT3Af7J2LhcEATBP2Ap7SkOM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:39+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" .
}