@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88130_assertion
;
np:hasProvenance
dgn-np:NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88130_provenance
;
np:hasPublicationInfo
dgn-np:NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88130_assertion
a
np:Assertion
.
dgn-np:NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88130_provenance
a
np:Provenance
.
dgn-np:NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88130_assertion
{
miriam-gene:6559
a
ncit:C16612
.
lld:C2931876
a
ncit:C7057
.
dgn-gda:DGN1e44fa8f46dd0a7711ec67bed5875211
sio:SIO_000628
miriam-gene:6559
,
lld:C2931876
;
a
sio:SIO_001121
.
}
dgn-np:NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88130_provenance
{
dgn-np:NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88130_assertion
dcterms:description
"[The objective of this review is to provide an overview of the pathophysiology and genetics of HSCR, within the context of our current knowledge of NCC development, sex chromosome genetics and laboratory models.]. 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:23043324
;
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:NP399201.RAWoovao1sWSO2L_clqU3_vqbGqvJ4s9RaIOT_Mqt5x88130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}