@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg
> .
@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:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_head
{
this:
np:hasAssertion
dgn-np:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_assertion
;
np:hasProvenance
dgn-np:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_provenance
;
np:hasPublicationInfo
dgn-np:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_assertion
a
np:Assertion
.
dgn-np:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_provenance
a
np:Provenance
.
dgn-np:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN44b92c927c94417022128cd4f1d9ed78
sio:SIO_000628
miriam-gene:4137
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_provenance
{
dgn-np:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_assertion
dcterms:description
"[These findings suggest that the H1/H2 polymorphism in MAPT is not associated with human amyotrophic lateral sclerosis, and that lowering tau levels in the mutant SOD1 mouse does not affect the motor neuron degeneration in these animals.]. 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:20498436
;
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:NP500778.RAqAPyWR4bMeTIwdHMbb06exTF3ogIgukkKbBK6u2FxUg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}