@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs
> .
@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:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_head
{
this:
np:hasAssertion
dgn-np:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_assertion
;
np:hasProvenance
dgn-np:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_provenance
;
np:hasPublicationInfo
dgn-np:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_assertion
a
np:Assertion
.
dgn-np:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_provenance
a
np:Provenance
.
dgn-np:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_assertion
{
miriam-gene:2317
a
ncit:C16612
.
lld:C0037932
a
ncit:C7057
.
dgn-gda:DGNf4b9f770f60155b35fdc329ddd1ea8fb
sio:SIO_000628
miriam-gene:2317
,
lld:C0037932
;
a
sio:SIO_001121
.
}
dgn-np:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_provenance
{
dgn-np:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_assertion
dcterms:description
"[Mice with loss of a single Cfm gene displayed no overt phenotype, whereas Cfm DKO mice showed skeletal malformations including spinal curvatures, vertebral fusions and impairment of bone growth, showing that the phenotypes of Cfm DKO mice resemble those of Filamin B (Flnb)-deficient mice.]. 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:24436304
;
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:NP407176.RAf30_ZgM-Sx9OPGEnY5-gDAQEin86NUDa8W9oAd_mERs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:37+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" .
}