@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4
> .
@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:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_head
{
this:
np:hasAssertion
dgn-np:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_assertion
;
np:hasProvenance
dgn-np:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_provenance
;
np:hasPublicationInfo
dgn-np:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_assertion
a
np:Assertion
.
dgn-np:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_provenance
a
np:Provenance
.
dgn-np:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_assertion
{
miriam-gene:642
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN693a3873adebb8eb04c29a95afbb14c1
sio:SIO_000628
miriam-gene:642
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_provenance
{
dgn-np:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_assertion
dcterms:description
"[To test this hypothesis, we examined this polymorphism in 621 rigorously evaluated patients and 502 control subjects (all caucasian) but were unable to detect an association between BH and AD even after controlling for age, gender, and apolipoprotein E (ApoE) genotype.]. 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:9818937
;
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:NP675972.RAibxNI6D_8bNrr5KKb9_XDe7h8FmTqxrN21T0zbupBB4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}