@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q
> .
@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:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_head
{
this:
np:hasAssertion
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_assertion
;
np:hasProvenance
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_assertion
a
np:Assertion
.
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_provenance
a
np:Provenance
.
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_assertion
{
miriam-gene:2263
a
ncit:C16612
.
lld:C0265269
a
ncit:C7057
.
dgn-gda:DGN2e923a97bccb889daac7f9abbb774226
sio:SIO_000628
miriam-gene:2263
,
lld:C0265269
;
a
sio:SIO_001121
.
}
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_provenance
{
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_assertion
dcterms:description
"[Moreover, the nearly identical conformation of WT FGFR2 kinase and the A628T LADD mutant to either the phosphorylated FGFR2 or FGFR2 harboring pathological activating mutations in the kinase hinge region suggests that FGFR autoinhibition and activation are better explained by changes in the conformational dynamics of the kinase rather than by static crystallographic snapshots of minor structural variations.]. 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:18056630
;
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:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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" .
}