@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y
> .
@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:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_head
{
this:
np:hasAssertion
dgn-np:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_assertion
;
np:hasProvenance
dgn-np:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_assertion
a
np:Assertion
.
dgn-np:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_provenance
a
np:Provenance
.
dgn-np:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_assertion
{
miriam-gene:283
a
ncit:C16612
.
lld:C1862939
a
ncit:C7057
.
dgn-gda:DGN05d49faf3c51ea2f17ae6cbe082dc038
sio:SIO_000628
miriam-gene:283
,
lld:C1862939
;
a
sio:SIO_001121
.
}
dgn-np:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_provenance
{
dgn-np:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_assertion
dcterms:description
"[Missense mutations in ANG gene have been identified in two ALS populations from Northern Europe and North America, both in familial (FALS) and sporadic (SALS) patients, but they do not seem to be frequent in the Italian population.]. 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:18087731
;
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:NP608677.RAmJ9QQsjpR2qekuTqMLtzuzfFFDNy6p1h8DWOgVqpE6Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}