@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og
> .
@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:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_head
{
this:
np:hasAssertion
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_assertion
;
np:hasProvenance
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_provenance
;
np:hasPublicationInfo
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_assertion
a
np:Assertion
.
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_provenance
a
np:Provenance
.
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_assertion
{
miriam-gene:7476
a
ncit:C16612
.
lld:C1856728
a
ncit:C7057
.
dgn-gda:DGNac4545e9ac45e131c68e2855e48c3af6
sio:SIO_000628
miriam-gene:7476
,
lld:C1856728
;
a
sio:SIO_001121
.
}
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_provenance
{
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_assertion
dcterms:description
"[Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel (AA/RRS) phocomelia syndrome are rare autosomal recessive inherited disorders characterized by aplastic/hypoplastic nails with ectopic dorsal palms, absence of humeri, hypoplastic ulnae, and bowed short radii with the elbow joints present, shown to result from missense mutations in WNT7A (p.Ala109Thr and p.Arg292Cys).]. 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:21344627
;
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:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:58+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" .
}