@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg
> .
@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:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_head
{
this:
np:hasAssertion
dgn-np:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_assertion
;
np:hasProvenance
dgn-np:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_provenance
;
np:hasPublicationInfo
dgn-np:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_assertion
a
np:Assertion
.
dgn-np:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_provenance
a
np:Provenance
.
dgn-np:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_assertion
{
miriam-gene:9856
a
ncit:C16612
.
lld:C0175702
a
ncit:C7057
.
dgn-gda:DGN4e8d0b83d0b2478f34bfdd5de2ce96ea
sio:SIO_000628
miriam-gene:9856
,
lld:C0175702
;
a
sio:SIO_001121
.
}
dgn-np:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_provenance
{
dgn-np:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_assertion
dcterms:description
"[These abnormalities are consistent with an alteration of the late stages of neuronal migration, define alterations of white matter structures underlying dissociable behavioral phenotypes in WS, and provide human in vivo information about genetic control of white matter tract formation.]. 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:17827280
;
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:NP751821.RAZtpbmsj-PcV9425BI4QL3QE_ngGGFK14uoev4Z4-mmg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:35+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" .
}