@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4
> .
@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:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_head
{
this:
np:hasAssertion
dgn-np:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_assertion
;
np:hasProvenance
dgn-np:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_provenance
;
np:hasPublicationInfo
dgn-np:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_assertion
a
np:Assertion
.
dgn-np:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_provenance
a
np:Provenance
.
dgn-np:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_assertion
{
miriam-gene:551
a
ncit:C16612
.
lld:C0687720
a
ncit:C7057
.
dgn-gda:DGNbef1177f9d1f51f626c554c881a0ac13
sio:SIO_000628
miriam-gene:551
,
lld:C0687720
;
a
sio:SIO_001121
.
}
dgn-np:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_provenance
{
dgn-np:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_assertion
dcterms:description
"[The disorder has a sex-linked recessive transmission, where all male offspring of an affected mother show the extreme thirst characteristic of the disease; in whom hyposthenuria persisted despite arginine vasopressin infusion, and in whom the serum arginine vasopressin concentrations correlate with the serum osmolality which serves to discriminate nephrogenic diabetes insipidus from the pituitary diabetes insipidus.]. 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:4093246
;
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:NP159065.RAMDzX9kf8hlI60yltSNYey9ZWzdcxKweWSlsDqBrUui4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}