@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8
> .
@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:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_head
{
this:
np:hasAssertion
dgn-np:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_assertion
;
np:hasProvenance
dgn-np:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_provenance
;
np:hasPublicationInfo
dgn-np:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_assertion
a
np:Assertion
.
dgn-np:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_provenance
a
np:Provenance
.
dgn-np:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_assertion
{
miriam-gene:1667
a
ncit:C16612
.
lld:C0268164
a
ncit:C7057
.
dgn-gda:DGN744a10b9bdb84732db254a667df4d44f
sio:SIO_000628
miriam-gene:1667
,
lld:C0268164
;
a
sio:SIO_001121
.
}
dgn-np:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_provenance
{
dgn-np:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_assertion
dcterms:description
"[The conflicting evidence on disease association and the lack of association between disease and particular populations, despite the wide range of HP(1) and HP(2) gene frequencies across the world, may indicate that any associations are marginal.]. 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:17474882
;
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:NP232099.RAA0YlB-EDYuKMRQ_D3LSu5qEs17fapZFwOkzUkBLSEI8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}