@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A
> .
@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:NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A130_assertion
;
np:hasProvenance
dgn-np:NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A130_provenance
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np:hasPublicationInfo
dgn-np:NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A130_assertion
a
np:Assertion
.
dgn-np:NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A130_provenance
a
np:Provenance
.
dgn-np:NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A130_assertion
{
miriam-gene:7289
a
ncit:C16612
.
lld:C0345354
a
ncit:C7057
.
dgn-gda:DGNbd4e8812c0cd25f30c583f86d9f9e3c6
sio:SIO_000628
miriam-gene:7289
,
lld:C0345354
;
a
sio:SIO_001121
.
}
dgn-np:NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A130_provenance
{
dgn-np:NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A130_assertion
dcterms:description
"[We have identified a new mouse mutant that is a strongly hypomorphic allele of Tulp3 and which exhibits expansion of ventral markers in the caudal spinal cord, as well as neural tube defects and preaxial polydactyly, consistent with increased Shh signalling.]. 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:19223390
;
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:NP641962.RAaXAc1aOvvu6otMIOYK1TJOAaXfFVk-96WsLAO46Un6A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:27+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
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"v2.1.0" .
}