@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc
> .
@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:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_head
{
this:
np:hasAssertion
dgn-np:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_assertion
;
np:hasProvenance
dgn-np:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_provenance
;
np:hasPublicationInfo
dgn-np:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_assertion
a
np:Assertion
.
dgn-np:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_provenance
a
np:Provenance
.
dgn-np:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_assertion
{
miriam-gene:5179
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN6c8ed19fac2ad3d1deeb133249776a68
sio:SIO_000628
miriam-gene:5179
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_provenance
{
dgn-np:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_assertion
dcterms:description
"[Northern blot analysis, using a single-stranded human proenkephalin A antisense probe (cRNA), revealed the existence of two different proenkephalin A-like sequences in the human caudate nucleus and pheochromocytoma RNA extracts of approximately 1400 and 1000 nucleotides in length respectively, whereas no specific RNA bands could be detected in the cortex and only the 1400 nucleotide band was present in the cerebellum.]. 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:3207862
;
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:NP856487.RAypXIWHcC-qGbmnJVCZIRxvzbucnp8ZBD-uiNNuPQ5tc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:43+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" .
}