@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg
> .
@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:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_head
{
this:
np:hasAssertion
dgn-np:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_assertion
;
np:hasProvenance
dgn-np:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_provenance
;
np:hasPublicationInfo
dgn-np:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_assertion
a
np:Assertion
.
dgn-np:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_provenance
a
np:Provenance
.
dgn-np:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_assertion
{
miriam-gene:2521
a
ncit:C16612
.
lld:C0338451
a
ncit:C7057
.
dgn-gda:DGN88690bd1af0700de9696502aba351dc2
sio:SIO_000628
miriam-gene:2521
,
lld:C0338451
;
a
sio:SIO_001121
.
}
dgn-np:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_provenance
{
dgn-np:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_assertion
dcterms:description
"[The link between RNA processing and ALS was further strengthened by the discovery that another genetic locus linking familial ALS (fALS) and FTD was due to mutation of the fused in sarcoma (FUS) gene.]. 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:22105541
;
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:NP300206.RAUvqFW04T0j4Dtq5TGOmT1ruj8nXn50lanwhhriHwjvg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}