@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco
> .
@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:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_head
{
this:
np:hasAssertion
dgn-np:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_assertion
;
np:hasProvenance
dgn-np:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_provenance
;
np:hasPublicationInfo
dgn-np:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_assertion
a
np:Assertion
.
dgn-np:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_provenance
a
np:Provenance
.
dgn-np:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_assertion
{
miriam-gene:6548
a
ncit:C16612
.
lld:C0267663
a
ncit:C7057
.
dgn-gda:DGN30c87204b6dce69c4bdbcbf6592a511b
sio:SIO_000628
miriam-gene:6548
,
lld:C0267663
;
a
sio:SIO_001121
.
}
dgn-np:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_provenance
{
dgn-np:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_assertion
dcterms:description
"[Homozygosity mapping and/or multipoint linkage analysis excluded the NHE1 locus on chromosome 1, NHE2 locus on chromosome 2, NHE3 locus on chromosome 5, and NHE5 locus on chromosome 16 as potential candidate genes for CSD in this pedigree.]. 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:11113072
;
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:NP307661.RAj-y4_9NH9BTFRmByZxdw3KH5UdbpXvRUUzViKGerXco130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}