@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw
> .
@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/v4.0.0/void/
> .
dgn-np:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_head
{
this:
np:hasAssertion
dgn-np:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_assertion
;
np:hasProvenance
dgn-np:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_provenance
;
np:hasPublicationInfo
dgn-np:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_assertion
a
np:Assertion
.
dgn-np:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_provenance
a
np:Provenance
.
dgn-np:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_assertion
{
miriam-gene:10083
a
ncit:C16612
.
lld:C1848604
a
ncit:C7057
.
dgn-gda:DGN5b6422792e6ce77648b24cd019bdd2c1
sio:SIO_000628
miriam-gene:10083
,
lld:C1848604
;
a
sio:SIO_001121
.
}
dgn-np:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_provenance
{
dgn-np:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_assertion
dcterms:description
"[Patients with Usher syndrome type IC can have the Acadian haplotype or the Lebanese haplotype compatible with the idea that at least two independently arising pathogenic mutations have occurred in the yet-to-be identified USH1C 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:11239869
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP310341.RA4_vhdy_rc1gemdz7a1VlCXl8pWWOBuGuSkTrQ15tCLw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:06+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}