@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY
> .
@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:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_head
{
this:
np:hasAssertion
dgn-np:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_assertion
;
np:hasProvenance
dgn-np:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_provenance
;
np:hasPublicationInfo
dgn-np:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_assertion
a
np:Assertion
.
dgn-np:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_provenance
a
np:Provenance
.
dgn-np:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_assertion
{
miriam-gene:53341
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGNe7e2699f90fe02f6957e4dd83d2fced8
sio:SIO_000628
miriam-gene:53341
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_provenance
{
dgn-np:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_assertion
dcterms:description
"[Another severe developmental defect that involves the brain is microhydranencephaly which manifests with microcephaly, motor and mental retardation and brain malformations that include gross dilation of the ventricles with complete absence of the cerebral hemispheres or severe delay in their development.]. 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:22526350
;
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:NP530411.RAYSRI6mT6kFBeIpHM1CHNu2CNI-FMRRWHXFkLwDUbyCY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:20+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" .
}