@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY
> .
@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:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_head
{
this:
np:hasAssertion
dgn-np:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_assertion
;
np:hasProvenance
dgn-np:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_provenance
;
np:hasPublicationInfo
dgn-np:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_assertion
a
np:Assertion
.
dgn-np:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_provenance
a
np:Provenance
.
dgn-np:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_assertion
{
miriam-gene:2778
a
ncit:C16612
.
lld:C0259779
a
ncit:C7057
.
dgn-gda:DGNca250534c917a199f74b0837d6d29849
sio:SIO_000628
miriam-gene:2778
,
lld:C0259779
;
a
sio:SIO_001121
.
}
dgn-np:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_provenance
{
dgn-np:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_assertion
dcterms:description
"[Results from the initial analysis of the series indicate five main points: (1) Significant diagnostic pitfalls affect the diagnosis of MFD and, to a lesser extent, PFD in orthopedic centers and allied radiology and pathology facilities, which may be circumvented by the adoption of stringent diagnostic criteria, and in some cases by the analysis of FD-associated GNAS1 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:12703030
;
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:NP158250.RAhYcU9kU73UJrfEdrokh39XVeuudK1682b1yStbKz8eY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:25+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" .
}