@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_head
{
this:
np:hasAssertion
dgn-np:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_assertion
;
np:hasProvenance
dgn-np:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_assertion
a
np:Assertion
.
dgn-np:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_provenance
a
np:Provenance
.
dgn-np:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_assertion
{
miriam-gene:2521
a
ncit:C16612
.
lld:C1862939
a
ncit:C7057
.
dgn-gda:DGNebae1c3f164172b36c48a5a69f1b2724
sio:SIO_000628
miriam-gene:2521
,
lld:C1862939
;
a
sio:SIO_001121
.
}
dgn-np:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_provenance
{
dgn-np:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_assertion
dcterms:description
"[This study defined the distribution and frequency of mutations of FALS in a Taiwanese Han Chinese population, which not only broadens the spectrum of the mutations causing FALS, but also further highlights the importance of FUS and TARDBP in the pathogenesis of amyotrophic lateral sclerosis (ALS).]. 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:20472325
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP812308.RAlU7O_g3_fLp9QPOZj7IDZsJ-c0LXUiQ3eJ42gYwx1GQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:53+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}