@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM
> .
@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:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_head
{
this:
np:hasAssertion
dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_assertion
;
np:hasProvenance
dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_provenance
;
np:hasPublicationInfo
dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_assertion
a
np:Assertion
.
dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_provenance
a
np:Provenance
.
dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_assertion
{
miriam-gene:5216
a
ncit:C16612
.
lld:C0236642
a
ncit:C7057
.
dgn-gda:DGN14b6a48d290ab796424cedeaf8795009
sio:SIO_000628
miriam-gene:5216
,
lld:C0236642
;
a
sio:SIO_001121
.
}
dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_provenance
{
dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_assertion
dcterms:description
"[Here, we performed a large screen of US, Nordic, and German familial and sporadic ALS and frontotemporal dementia (FTLD) patients for PFN1 mutations to get further insight into the spectrum and pathogenic relevance of this gene for the complete ALS/FTLD continuum.]. 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:23141414
;
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:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}