@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_head
{
this:
np:hasAssertion
dgn-np:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_assertion
;
np:hasProvenance
dgn-np:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_assertion
a
np:Assertion
.
dgn-np:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_provenance
a
np:Provenance
.
dgn-np:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_assertion
{
miriam-gene:65057
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN32af762a8dac01323c941ecfaaa9d78e
sio:SIO_000628
miriam-gene:65057
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_provenance
{
dgn-np:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_assertion
dcterms:description
"[Understanding the clinical spectrum of ACD and the cloning of an 'ACD gene' both have implications for counseling, for prenatal testing, and for understanding the molecular pathophysiology of ACD and other organ malformations that are associated with this condition.]. 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:15520767
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP940665.RAAcuP5-PeNwSCOJF6zMbjnLc-jr11dr-utRXUlY81rEQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:14+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}