@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE
> .
@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:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_head
{
this:
np:hasAssertion
dgn-np:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_assertion
;
np:hasProvenance
dgn-np:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_provenance
;
np:hasPublicationInfo
dgn-np:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_assertion
a
np:Assertion
.
dgn-np:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_provenance
a
np:Provenance
.
dgn-np:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0027404
a
ncit:C7057
.
dgn-gda:DGN5f316111f2160ebde0bafbcd7cf7d660
sio:SIO_000628
miriam-gene:3126
,
lld:C0027404
;
a
sio:SIO_001121
.
}
dgn-np:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_provenance
{
dgn-np:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_assertion
dcterms:description
"[We explored the role of hypocretins in human narcolepsy through histopathology of six narcolepsy brains and mutation screening of Hcrt, Hcrtr1 and Hcrtr2 in 74 patients of various human leukocyte antigen and family history status.]. 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:10973318
;
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:NP486665.RA8qsEVnmQtMKoo5bwGJmROGo6IMo-sbVNTkbcGXo9LJE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}