@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA
> .
@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:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_head
{
this:
np:hasAssertion
dgn-np:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_assertion
;
np:hasProvenance
dgn-np:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_provenance
;
np:hasPublicationInfo
dgn-np:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_assertion
a
np:Assertion
.
dgn-np:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_provenance
a
np:Provenance
.
dgn-np:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_assertion
{
miriam-gene:8181
a
ncit:C16612
.
lld:C0220669
a
ncit:C7057
.
dgn-gda:DGN1039be66487ebdadf5ec3823cc720a19
sio:SIO_000628
miriam-gene:8181
,
lld:C0220669
;
a
sio:SIO_001121
.
}
dgn-np:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_provenance
{
dgn-np:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_assertion
dcterms:description
"[In all analyzed families, we found no evidence for linkage to the BFIC loci on chromosomes 19q and 2q, as well as to the known loci for benign familial neonatal convulsions on chromosomes 8q and 20q.]. 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:15144424
;
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:NP521353.RAGYv6VraxN2f2N6nnDmTQP5w8NtqnF1JA40obWxI-AGA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}