@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc
> .
@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:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_head
{
this:
np:hasAssertion
dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_assertion
;
np:hasProvenance
dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_provenance
;
np:hasPublicationInfo
dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_assertion
a
np:Assertion
.
dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_provenance
a
np:Provenance
.
dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_assertion
{
miriam-gene:3557
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNa1526dd551703e9223af1a125610f21f
sio:SIO_000628
miriam-gene:3557
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_provenance
{
dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_assertion
dcterms:description
"[Despite the multiple hypotheses tested, the robustness of family design to population confoundings and the consistency with previous findings increase the likelihood of true association. Further investigation using larger data sets is needed in order for this to be confirmed. See the related commentary by Keavney: http://www.biomedcentral.com/1741-7015/8/6.]. 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:20070880
;
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:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:35+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" .
}