@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA
> .
@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/v4.0.0/void/
> .
dgn-np:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_head
{
this:
np:hasAssertion
dgn-np:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_assertion
;
np:hasProvenance
dgn-np:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_provenance
;
np:hasPublicationInfo
dgn-np:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_assertion
a
np:Assertion
.
dgn-np:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_provenance
a
np:Provenance
.
dgn-np:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_assertion
{
miriam-gene:2263
a
ncit:C16612
.
lld:C2931196
a
ncit:C7057
.
dgn-gda:DGN4bf8f6ca93d326d6676608a0c298f29d
sio:SIO_000628
miriam-gene:2263
,
lld:C2931196
;
a
sio:SIO_001121
.
}
dgn-np:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_provenance
{
dgn-np:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_assertion
dcterms:description
"[Genotype-phenotype analyses based on our cohort and previous studies further indicate that in spite of some overlap, PS and CS are preferentially accounted for by two distinct sets of FGFR2 mutations.]. 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:16418739
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP531466.RAckGnr3SP_Oc4k4YxXJIanP_NdGfjqvCOcGTQCJ91jQA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:45+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}