@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg
> .
@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:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_head
{
this:
np:hasAssertion
dgn-np:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_assertion
;
np:hasProvenance
dgn-np:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_provenance
;
np:hasPublicationInfo
dgn-np:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_assertion
a
np:Assertion
.
dgn-np:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_provenance
a
np:Provenance
.
dgn-np:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_assertion
{
miriam-gene:7291
a
ncit:C16612
.
lld:C0410528
a
ncit:C7057
.
dgn-gda:DGN59754fec6ad2a77a182d9aa97952c2fd
sio:SIO_000628
miriam-gene:7291
,
lld:C0410528
;
a
sio:SIO_001121
.
}
dgn-np:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_provenance
{
dgn-np:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_assertion
dcterms:description
"[However, more direct evidence for abnormal tyrosine kinase receptor signalling in AN has been provided by studies of craniosynostosis and skeletal dysplasia syndromes with AN, which have identified activating mutations in fibroblast growth factor receptors.]. 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:12452857
;
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:NP733791.RArR1rbvP_kOx9Gw4tPTSLAfLzCSae9u07GRdPa2W94Mg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:25+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" .
}