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http://rdf.disgenet.org/nanopublications.trig#NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio130_assertion
;
np:hasProvenance
dgn-np:NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio130_provenance
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np:hasPublicationInfo
dgn-np:NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio130_assertion
a
np:Assertion
.
dgn-np:NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio130_provenance
a
np:Provenance
.
dgn-np:NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio130_assertion
{
miriam-gene:1641
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGNc2ffa82c796a7b1a1cbd45b8657ef5a0
sio:SIO_000628
miriam-gene:1641
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio130_provenance
{
dgn-np:NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio130_assertion
dcterms:description
"[Whereas the brain malformation due to LIS1 mutations was more severe over the parietal and occipital regions, XLIS mutations produced the reverse gradient, which was more severe over the frontal cortex.]. 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:9817918
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
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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 .
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dgn-np:NP931184.RAUplXvwY2vgC1RCVOspBtSiHzBpCzUk9bwAccSvJIYio130_publicationInfo
{
this:
dcterms:created
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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
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pav:authoredBy
<
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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pav:version
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