@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8
> .
@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:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_head
{
this:
np:hasAssertion
dgn-np:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_assertion
;
np:hasProvenance
dgn-np:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_provenance
;
np:hasPublicationInfo
dgn-np:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_assertion
a
np:Assertion
.
dgn-np:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_provenance
a
np:Provenance
.
dgn-np:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_assertion
{
miriam-gene:6010
a
ncit:C16612
.
lld:C0339535
a
ncit:C7057
.
dgn-gda:DGN0f2ba2d1b65de65f77c77b9829f79f51
sio:SIO_000628
miriam-gene:6010
,
lld:C0339535
;
a
sio:SIO_001121
.
}
dgn-np:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_provenance
{
dgn-np:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_assertion
dcterms:description
"[We have excluded the five previously known mutations in the three genes (RHO, PDE6B and GNAT1) associated with adCSNB, and linkage studies have excluded tight linkage between the disease locus and markers associated with these three genes.]. 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:15845035
;
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:NP766157.RADAUNDgPd_pRO5a6IoUloi_a2hh67BVMV_cL7F-AF4-8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}