@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU
> .
@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:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_head
{
this:
np:hasAssertion
dgn-np:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_assertion
;
np:hasProvenance
dgn-np:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_provenance
;
np:hasPublicationInfo
dgn-np:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_assertion
a
np:Assertion
.
dgn-np:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_provenance
a
np:Provenance
.
dgn-np:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_assertion
{
miriam-gene:11081
a
ncit:C16612
.
lld:C1857574
a
ncit:C7057
.
dgn-gda:DGNe0436cebfe20abba7b36753090a5987d
sio:SIO_000628
miriam-gene:11081
,
lld:C1857574
;
a
sio:SIO_001121
.
}
dgn-np:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_provenance
{
dgn-np:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_assertion
dcterms:description
"[We also studied 22 single nucleotide polymorphisms distributed in the KERA genomic region by direct sequencing in this family as well as in one additional Finnish patient with CNA2 and 24 white British control subjects.]. 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:17679937
;
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:NP627564.RAngRg-y34zboqIaAWkhV0ULt1vx5_ImmmPEr91W3Y9dU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:18+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" .
}