@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY
> .
@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:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_head
{
this:
np:hasAssertion
dgn-np:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_assertion
;
np:hasProvenance
dgn-np:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_provenance
;
np:hasPublicationInfo
dgn-np:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_assertion
a
np:Assertion
.
dgn-np:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_provenance
a
np:Provenance
.
dgn-np:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN4743e418c1ab77079fa67752d3536a56
sio:SIO_000628
miriam-gene:3918
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_provenance
{
dgn-np:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_assertion
dcterms:description
"[Logistic regression analysis supported race, anemia, body mass index, and male gender as independent risk factors for severe visual loss and suggested that racial differences may be partially accounted for by differences in CSF opening pressure, body mass index, and frequency of anemia.]. 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:18332344
;
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:NP716784.RAbSeO1SUipaWVmRQxyEwngbD0x07ChMi6r5Xjw9pLiRY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:15+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" .
}