@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao
> .
@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:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_head
{
this:
np:hasAssertion
dgn-np:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_assertion
;
np:hasProvenance
dgn-np:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_provenance
;
np:hasPublicationInfo
dgn-np:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_assertion
a
np:Assertion
.
dgn-np:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_provenance
a
np:Provenance
.
dgn-np:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_assertion
{
miriam-gene:3842
a
ncit:C16612
.
lld:C1858679
a
ncit:C7057
.
dgn-gda:DGN17e4df9fd3e1f8e786e3bb63269a1b43
sio:SIO_000628
miriam-gene:3842
,
lld:C1858679
;
a
sio:SIO_001121
.
}
dgn-np:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_provenance
{
dgn-np:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_assertion
dcterms:description
"[To further elucidate the cataract phenotype, and identify the gene and mutation for autosomal dominant cataract (ADC) in an American family of European descent (ADC2) by sequencing the major intrinsic protein gene (MIP), a candidate based on linkage to chromosome 12q13.]. 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:16564824
;
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:NP257979.RA0BbCJctDo2curzJTq6pnJBqpp71rbno0WtQCZ0MKSao130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:24+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" .
}