@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0
> .
@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:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_head
{
this:
np:hasAssertion
dgn-np:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_assertion
;
np:hasProvenance
dgn-np:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_provenance
;
np:hasPublicationInfo
dgn-np:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_assertion
a
np:Assertion
.
dgn-np:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_provenance
a
np:Provenance
.
dgn-np:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_assertion
{
miriam-gene:9619
a
ncit:C16612
.
lld:C0027404
a
ncit:C7057
.
dgn-gda:DGN06430e1906b0503f530ae081a0241bcc
sio:SIO_000628
miriam-gene:9619
,
lld:C0027404
;
a
sio:SIO_001121
.
}
dgn-np:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_provenance
{
dgn-np:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_assertion
dcterms:description
"[A single haplotype was shared by all affected individuals and informative crossovers indicated that the elusive gene that confers susceptibility to narcolepsy is likely to be located between markers D21S267 and ABCG1, in a 5.15 Mb region of 21q.]. 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:15349865
;
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:NP512756.RAif7bHbeTEGNdzkhvIRrAKRgsUi6hJjghpDCfH0_fPA0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}