@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A
> .
@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:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_head
{
this:
np:hasAssertion
dgn-np:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_assertion
;
np:hasProvenance
dgn-np:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_provenance
;
np:hasPublicationInfo
dgn-np:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_assertion
a
np:Assertion
.
dgn-np:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_provenance
a
np:Provenance
.
dgn-np:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_assertion
{
miriam-gene:90
a
ncit:C16612
.
lld:C0016037
a
ncit:C7057
.
dgn-gda:DGN5fc81e7984917ef0bf4caccd80081824
sio:SIO_000628
miriam-gene:90
,
lld:C0016037
;
a
sio:SIO_001121
.
}
dgn-np:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_provenance
{
dgn-np:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_assertion
dcterms:description
"[Although the genetic defects of FOP are not completely known, several clinical and animal model studies have implicated that mutations in bone morphogenetic proteins, their receptors, and activin receptor type IA (ACVR1) genes are associated with FOP primarily.]. 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:23229308
;
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:NP222205.RAI7NMY5isDuEHzuPTyyXL2-9Vq0BArLzfLJTMi0m1i7A130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:46+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" .
}