@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI
> .
@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:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_head
{
this:
np:hasAssertion
dgn-np:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_assertion
;
np:hasProvenance
dgn-np:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_provenance
;
np:hasPublicationInfo
dgn-np:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_assertion
a
np:Assertion
.
dgn-np:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_provenance
a
np:Provenance
.
dgn-np:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_assertion
{
miriam-gene:1728
a
ncit:C16612
.
lld:C0220726
a
ncit:C7057
.
dgn-gda:DGN7cc1b1330f0590105a1e6057ba5051c3
sio:SIO_000628
miriam-gene:1728
,
lld:C0220726
;
a
sio:SIO_001121
.
}
dgn-np:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_provenance
{
dgn-np:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_assertion
dcterms:description
"[Using these methods, we report striking linkage disequilibrium for diastrophic dysplasia (DTD) in Finland indicating that the DTD gene should lie within 0.06 centimorgans (or about 60 kilobases) of the CSF1R 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:1345170
;
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:NP708951.RARnZVfeGXdkGvin8uOcWShbsRtBWulPSzbusZNj9UPvI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}