@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM
> .
@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:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_head
{
this:
np:hasAssertion
dgn-np:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_assertion
;
np:hasProvenance
dgn-np:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_provenance
;
np:hasPublicationInfo
dgn-np:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_assertion
a
np:Assertion
.
dgn-np:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_provenance
a
np:Provenance
.
dgn-np:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_assertion
{
miriam-gene:4487
a
ncit:C16612
.
lld:C0426980
a
ncit:C7057
.
dgn-gda:DGN0c2b52bd0b9095f409c8b6f7f81139a5
sio:SIO_000628
miriam-gene:4487
,
lld:C0426980
;
a
sio:SIO_001121
.
}
dgn-np:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_provenance
{
dgn-np:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_assertion
dcterms:description
"[We used data from 535 HD participants of the New England Huntington cohort and the HD MAPS cohort to assess whether AO was influenced by any of the three markers in the 4p16 region: MSX1 (Drosophila homeo box homologue 1, formerly known as homeo box 7, HOX7), Delta2642 (within the HD coding sequence), and BJ56 ( D4S127).]. 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:15029481
;
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:NP311526.RAM555bEFCfGY3MA5u0rGaBfu5kl9hqvHOkjmsjSBQsFM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:58+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" .
}