@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg
> .
@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:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_head
{
this:
np:hasAssertion
dgn-np:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_assertion
;
np:hasProvenance
dgn-np:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_provenance
;
np:hasPublicationInfo
dgn-np:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_assertion
a
np:Assertion
.
dgn-np:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_provenance
a
np:Provenance
.
dgn-np:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_assertion
{
miriam-gene:3356
a
ncit:C16612
.
lld:C0035335
a
ncit:C7057
.
dgn-gda:DGN307bfc8d1f218ea11e918f5b4a291426
sio:SIO_000628
miriam-gene:3356
,
lld:C0035335
;
a
sio:SIO_001121
.
}
dgn-np:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_provenance
{
dgn-np:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_assertion
dcterms:description
"[These results suggest that the human HTR2 gene might be affected by genomic imprinting and that exclusive expression of the maternal HTR2 gene may be associated with the delayed occurrence of RB, which had lost the maternal chromosome 13.]. 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:8900237
;
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:NP430138.RA8l9P-Qky7o3l8rLLViVMgz9RLjZWI0LGkQDLKs9KTUg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}