@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok
> .
@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:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_head
{
this:
np:hasAssertion
dgn-np:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_assertion
;
np:hasProvenance
dgn-np:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_provenance
;
np:hasPublicationInfo
dgn-np:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_assertion
a
np:Assertion
.
dgn-np:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_provenance
a
np:Provenance
.
dgn-np:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_assertion
{
miriam-gene:7700
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN6d4463fab08260f569bb5376c783c91d
sio:SIO_000628
miriam-gene:7700
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_provenance
{
dgn-np:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_assertion
dcterms:description
"[Allelic frequencies of RFLPs at loci closely linked to the HD gene, D4S95, D4S91, D4S141, and D4S90, were determined in 13 Huntington's disease (HD) patients from nine Chinese families and 129 normal subjects.]. 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:7760321
;
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:NP910381.RA2qs0UBVXovfIJSdSqwtOJDZywVkXPSx3M1CwKg7JZok130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}