@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA
> .
@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:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_head
{
this:
np:hasAssertion
dgn-np:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_assertion
;
np:hasProvenance
dgn-np:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_provenance
;
np:hasPublicationInfo
dgn-np:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_assertion
a
np:Assertion
.
dgn-np:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_provenance
a
np:Provenance
.
dgn-np:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0338451
a
ncit:C7057
.
dgn-gda:DGN5a91071efe35be1967452005da28c378
sio:SIO_000628
miriam-gene:1437
,
lld:C0338451
;
a
sio:SIO_001121
.
}
dgn-np:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_provenance
{
dgn-np:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_assertion
dcterms:description
"[Their relative abundance, functional significance, and secretion into the cerebrospinal fluid (CSF), saliva, and the general circulation have made granins tractable targets as biomarkers for many diseases of neuronal and endocrine origin, recently impacting diagnosis of a number of neurological and psychiatric disorders including amyotrophic lateral sclerosis (ALS), Alzheimer's disease, frontotemporal dementia, and schizophrenia.]. 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:20600637
;
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:NP501838.RAVh2A7iGYd9XnAvXrcMxL4rByup9VgvhEeoRDUK_ZvFA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}