@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY
> .
@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:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_head
{
this:
np:hasAssertion
dgn-np:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_assertion
;
np:hasProvenance
dgn-np:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_provenance
;
np:hasPublicationInfo
dgn-np:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_assertion
a
np:Assertion
.
dgn-np:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_provenance
a
np:Provenance
.
dgn-np:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0041696
a
ncit:C7057
.
dgn-gda:DGN2b01fe945f08add181b4ba8f0f5293eb
sio:SIO_000628
miriam-gene:3918
,
lld:C0041696
;
a
sio:SIO_001121
.
}
dgn-np:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_provenance
{
dgn-np:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_assertion
dcterms:description
"[Regardless of the mechanisms (altered synthesis/release/metabolism in brain or changed fate in CSF) leading to elevated CSF CGRP-LI, the identification of a possible disease trait marker should contribute to the early diagnosis of major depression and identification of family members at risk and may help in differential diagnosis in other disorders with affective symptomatology.]. 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:7715797
;
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:NP573428.RANqEWyltXNIA6nnrFwo-4oCxSK3J0FlIInvlmvgzYllY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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" .
}