@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q
> .
@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:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_head
{
this:
np:hasAssertion
dgn-np:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_assertion
;
np:hasProvenance
dgn-np:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_assertion
a
np:Assertion
.
dgn-np:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_provenance
a
np:Provenance
.
dgn-np:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_assertion
{
miriam-gene:1896
a
ncit:C16612
.
lld:C0162359
a
ncit:C7057
.
dgn-gda:DGNa540b721259e996153a28794f5a18adc
sio:SIO_000628
miriam-gene:1896
,
lld:C0162359
;
a
sio:SIO_001121
.
}
dgn-np:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_provenance
{
dgn-np:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_assertion
dcterms:description
"[The absence of recombination between EDA and the DXS732 locus lends support to the hypothesis that the DXCrc169 locus in the mouse and the DXS732 locus in humans may contain candidate sequences for the Ta and EDA genes, respectively.]. 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:1357963
;
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:NP173779.RAPGWRS4dDcphqoAylGmIwMtQMrbIzzx9zhIwTB0Ri31Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}