@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc
> .
@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:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_head
{
this:
np:hasAssertion
dgn-np:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_assertion
;
np:hasProvenance
dgn-np:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_provenance
;
np:hasPublicationInfo
dgn-np:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_assertion
a
np:Assertion
.
dgn-np:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_provenance
a
np:Provenance
.
dgn-np:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_assertion
{
miriam-gene:1270
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN1f10fb29d82027cb0e2c0c2be0e56722
sio:SIO_000628
miriam-gene:1270
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_provenance
{
dgn-np:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_assertion
dcterms:description
"[Using this method, CNTF levels were determined in human sciatic nerves obtained at autopsy from 21 amyotrophic lateral sclerosis (ALS) patients and 48 subjects who had died of other neurological diseases.]. 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:8764576
;
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:NP778968.RA2skcLCpuHfJmyYos9osxtgcrQULG_LCCNh8itoRVRyc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:52+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" .
}