@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0
> .
@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:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_head
{
this:
np:hasAssertion
dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_assertion
;
np:hasProvenance
dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_provenance
;
np:hasPublicationInfo
dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_assertion
a
np:Assertion
.
dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_provenance
a
np:Provenance
.
dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_assertion
{
miriam-gene:4763
a
ncit:C16612
.
lld:C0027765
a
ncit:C7057
.
dgn-gda:DGNa78aa4d5a03826120cb47871897e3ad4
sio:SIO_000628
miriam-gene:4763
,
lld:C0027765
;
a
sio:SIO_001121
.
}
dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_provenance
{
dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_assertion
dcterms:description
"[The molecular defects responsible for Huntington's disease, the spinocerebellar degenerations, myotonic muscular dystrophy, neurofibromatosis, and tuberous sclerosis, among other major dominant inherited diseases of the nervous system, will be identified using the new techniques of molecular genetics.]. 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:6378063
;
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:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}