@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI
> .
@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 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:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_head
{
this:
np:hasAssertion
dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_assertion
;
np:hasProvenance
dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_provenance
;
np:hasPublicationInfo
dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_assertion
a
np:Assertion
.
dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_provenance
a
np:Provenance
.
dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_assertion
{
miriam-gene:2155
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNb5b29fcbc6d881dd215ed98462970f4f
sio:SIO_000628
miriam-gene:2155
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_provenance
{
dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_assertion
dct:description
"[This study shows that for some genes, further studies are unnecessary, whereas for others, no more enrollments are needed. The impact of certain genotypes must be examined in relation to other established risk factors and potentially new therapeutic strategies.]. 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:11397354
;
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:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}