@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo
> .
@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:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_head
{
this:
np:hasAssertion
dgn-np:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_assertion
;
np:hasProvenance
dgn-np:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_provenance
;
np:hasPublicationInfo
dgn-np:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_assertion
a
np:Assertion
.
dgn-np:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_provenance
a
np:Provenance
.
dgn-np:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_assertion
{
miriam-gene:4914
a
ncit:C16612
.
lld:C0000889
a
ncit:C7057
.
dgn-gda:DGNbd75a0aa55469b90f6038ca73b2703be
sio:SIO_000628
miriam-gene:4914
,
lld:C0000889
;
a
sio:SIO_001121
.
}
dgn-np:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_provenance
{
dgn-np:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_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-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:NP599664.RAhYqtD4hfLeA3gb2IeW3i1Y0HMMNPVJKZBwXT6baZuyo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:38+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" .
}