@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_head
{
this:
np:hasAssertion
dgn-np:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_assertion
;
np:hasProvenance
dgn-np:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_provenance
;
np:hasPublicationInfo
dgn-np:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_assertion
a
np:Assertion
.
dgn-np:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_provenance
a
np:Provenance
.
dgn-np:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_assertion
{
miriam-gene:7275
a
ncit:C16612
.
lld:C0339526
a
ncit:C7057
.
dgn-gda:DGN500397fdb182e5702ae836bc30fad76e
sio:SIO_000628
miriam-gene:7275
,
lld:C0339526
;
a
sio:SIO_001121
.
}
dgn-np:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_provenance
{
dgn-np:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_assertion
dcterms:description
"[A mutation screen of the entire coding region of the TUB gene in 159 unrelated patients with autosomal recessive RP, 114 unrelated patients with simplex RP, and 21 unrelated patients with LCA uncovered 18 sequence variations.]. 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:16643894
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP761514.RA66YNEN21PLpASkshVzD66ng2Lj_lO-8M_LQEO69mMTw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:19+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}