@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc
> .
@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:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_head
{
this:
np:hasAssertion
dgn-np:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_assertion
;
np:hasProvenance
dgn-np:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_provenance
;
np:hasPublicationInfo
dgn-np:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_assertion
a
np:Assertion
.
dgn-np:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_provenance
a
np:Provenance
.
dgn-np:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_assertion
{
miriam-gene:7979
a
ncit:C16612
.
lld:C0020725
a
ncit:C7057
.
dgn-gda:DGN6e86f867d105aee808e7779ef1e833ab
sio:SIO_000628
miriam-gene:7979
,
lld:C0020725
;
a
sio:SIO_001121
.
}
dgn-np:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_provenance
{
dgn-np:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_assertion
dcterms:description
"[These observations were consistent with differing mechanisms of action and modes of inheritance of ICD and ECD mutations, suggesting that individuals with an ECD mutation may require additional defect(s) for expression of CSS.]. 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:9927496
;
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:NP866917.RAGsyIMcllJs8uyfI7j7nmx5eN-5YtFoWFapC5DjnW2Cc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:50+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" .
}