@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ
> .
@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:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_head
{
this:
np:hasAssertion
dgn-np:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_assertion
;
np:hasProvenance
dgn-np:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_assertion
a
np:Assertion
.
dgn-np:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_provenance
a
np:Provenance
.
dgn-np:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_assertion
{
miriam-gene:23385
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN79dc3e17bba0b205c10afb8b5fae95c7
sio:SIO_000628
miriam-gene:23385
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_provenance
{
dgn-np:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_assertion
dcterms:description
"[We found some differences in the distribution of genotype alterations in the AD population compared to the controls. However, our data together with other evidence did not support the pathological role of missense mutation N417Y.]. 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:14642438
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP62169.RAXF7GgU7LM6IwpnxMxfoM4Za7NfVJ222Z-owz_t01USQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}