@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI
> .
@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:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_head
{
this:
np:hasAssertion
dgn-np:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_assertion
;
np:hasProvenance
dgn-np:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_assertion
a
np:Assertion
.
dgn-np:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_provenance
a
np:Provenance
.
dgn-np:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_assertion
{
miriam-gene:9856
a
ncit:C16612
.
lld:C0266463
a
ncit:C7057
.
dgn-gda:DGN4bf0d5966ed38d1c4b8188da6b7c6c80
sio:SIO_000628
miriam-gene:9856
,
lld:C0266463
;
a
sio:SIO_001121
.
}
dgn-np:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_provenance
{
dgn-np:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_assertion
dcterms:description
"[Detailed classification of brain malformations such as lissencephaly has led to the positional cloning of genes required for normal neuronal migration and the identification of unique molecular pathways governing brain structure.]. 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:11748497
;
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:NP321157.RADb0be2vLWRi7xOEdq7UjFyywu4AG73m-80spVUv9yYI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:06+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" .
}