@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY
> .
@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:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_head
{
this:
np:hasAssertion
dgn-np:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_assertion
;
np:hasProvenance
dgn-np:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_provenance
;
np:hasPublicationInfo
dgn-np:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_assertion
a
np:Assertion
.
dgn-np:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_provenance
a
np:Provenance
.
dgn-np:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_assertion
{
miriam-gene:7700
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN294d3f47b8e191d5782881e30567ac63
sio:SIO_000628
miriam-gene:7700
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_provenance
{
dgn-np:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_assertion
dcterms:description
"[These data suggest that it may be possible to construct high and low risk haplotypes, which may be helpful in DNA analysis and genetic counselling for HD, and represent independent evidence that the gene for HD is centromeric to more distally located DNA markers such as D4S90.]. 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:2531224
;
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:NP801613.RAXgwGEZI7Xsvcv3rYmdwOhiW_QXOlFc0JqnDEnbMaAlY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}