@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo
> .
@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:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_head
{
this:
np:hasAssertion
dgn-np:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_assertion
;
np:hasProvenance
dgn-np:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_provenance
;
np:hasPublicationInfo
dgn-np:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_assertion
a
np:Assertion
.
dgn-np:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_provenance
a
np:Provenance
.
dgn-np:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_assertion
{
miriam-gene:84976
a
ncit:C16612
.
lld:C2675857
a
ncit:C7057
.
dgn-gda:DGNccecb5201f949e7c4795ce6b9e0aed8f
sio:SIO_000628
miriam-gene:84976
,
lld:C2675857
;
a
sio:SIO_001121
.
}
dgn-np:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_provenance
{
dgn-np:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_assertion
dcterms:description
"[We performed an extensive mutational analysis of the entire human DISP1 gene, required for secretion of all hedgehog ligand(s) and which maps to the HPE 10 locus of human chromosome 1q41, as a HPE candidate gene.]. 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:19184110
;
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:NP267138.RA1FojXN6NcEIn-xzIgREZv_hCS1Eh2ZaJYxlB-vd9Rfo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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" .
}