@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ
> .
@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:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_head
{
this:
np:hasAssertion
dgn-np:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_assertion
;
np:hasProvenance
dgn-np:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_assertion
a
np:Assertion
.
dgn-np:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance
a
np:Provenance
.
dgn-np:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_assertion
{
miriam-gene:283297
a
ncit:C16612
.
lld:C0268164
a
ncit:C7057
.
dgn-gda:DGN20435076a662c8a8d959c99eb01745df
sio:SIO_000628
miriam-gene:283297
,
lld:C0268164
;
a
sio:SIO_001121
.
}
dgn-np:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_provenance
{
dgn-np:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_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:NP917869.RAmqzdR2r0wEnZy83iWM5VsJrqF2_7aHFgciH5y1_1axQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}