@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc
> .
@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:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_head
{
this:
np:hasAssertion
dgn-np:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_assertion
;
np:hasProvenance
dgn-np:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_provenance
;
np:hasPublicationInfo
dgn-np:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_assertion
a
np:Assertion
.
dgn-np:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_provenance
a
np:Provenance
.
dgn-np:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_assertion
{
miriam-gene:114327
a
ncit:C16612
.
lld:C0014553
a
ncit:C7057
.
dgn-gda:DGN6c7c56adde05d9d85247150088be6c00
sio:SIO_000628
miriam-gene:114327
,
lld:C0014553
;
a
sio:SIO_001121
.
}
dgn-np:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_provenance
{
dgn-np:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_assertion
dcterms:description
"[Our latest studies, as well as those by Whitehouse et al., show that not all families with JME have their genetic locus in chromosome 6p, and that childhood absence epilepsy does not map to the same EJM1 locus.]. 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:8293722
;
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:NP764982.RA7g7ZZ2w2QSBSC8uM6sz1l6F9LEdzlUhnA9TALL9YDtc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}