@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw
> .
@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:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_head
{
this:
np:hasAssertion
dgn-np:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_assertion
;
np:hasProvenance
dgn-np:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_provenance
;
np:hasPublicationInfo
dgn-np:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_assertion
a
np:Assertion
.
dgn-np:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_provenance
a
np:Provenance
.
dgn-np:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_assertion
{
miriam-gene:4744
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN5776c8dbbb7ab045628dd4cef7504ce0
sio:SIO_000628
miriam-gene:4744
,
lld:C0002736
;
a
sio:SIO_001122
.
}
dgn-np:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_provenance
{
dgn-np:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_assertion
dcterms:description
"[mutations in neurofilaments are possible risk factors that may contribute to pathogenesis in amyotrophic lateral sclerosis in conjunction with one or more additional genetic or environmental factors, but are not significant primary causes ]. 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:16084104
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP140692.RA4gnKDpxMALbjHQy9cyB9HwgU2uTzV7WpbChVEXFuDUw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:13+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" .
}