@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk
> .
@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:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_head
{
this:
np:hasAssertion
dgn-np:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_assertion
;
np:hasProvenance
dgn-np:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_provenance
;
np:hasPublicationInfo
dgn-np:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_assertion
a
np:Assertion
.
dgn-np:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_provenance
a
np:Provenance
.
dgn-np:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0019569
a
ncit:C7057
.
dgn-gda:DGN5f0a1218278b4742a7483c4882b34363
sio:SIO_000628
miriam-gene:5979
,
lld:C0019569
;
a
sio:SIO_001121
.
}
dgn-np:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_provenance
{
dgn-np:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_assertion
dcterms:description
"[RET is a candidate gene for IHPS due to its role in the development of the intrinsic innervation and ganglia of the smooth musculature and the association of RET variants with another motility disorder (Hirschsprung's disease).]. 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:22169991
;
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:NP283093.RA8Dp4IB-QVDh_yVKnX2pQ9y4PVK814mZkObo43hwNMLk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}