@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo
> .
@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:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_head
{
this:
np:hasAssertion
dgn-np:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_assertion
;
np:hasProvenance
dgn-np:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_provenance
;
np:hasPublicationInfo
dgn-np:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_assertion
a
np:Assertion
.
dgn-np:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_provenance
a
np:Provenance
.
dgn-np:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_assertion
{
miriam-gene:7415
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGNb1f703d7e58e6612faf586a94b1f8b87
sio:SIO_000628
miriam-gene:7415
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_provenance
{
dgn-np:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_assertion
dcterms:description
"[More recently, mutations in the valosin-containing protein (VCP) gene linked to the human genetic disease, Inclusion Body Myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD), were found also to be associated with ALS in some patients.]. 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:22898872
;
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:NP197467.RA6pp4WutuapTwzoauxwryXcEiAE_Sx0nA19d8UBRNdNo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}