@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY
> .
@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:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_head
{
this:
np:hasAssertion
dgn-np:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_assertion
;
np:hasProvenance
dgn-np:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_provenance
;
np:hasPublicationInfo
dgn-np:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_assertion
a
np:Assertion
.
dgn-np:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_provenance
a
np:Provenance
.
dgn-np:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_assertion
{
miriam-gene:2006
a
ncit:C16612
.
lld:C0019825
a
ncit:C7057
.
dgn-gda:DGN089027de25af047f8d8808659819e797
sio:SIO_000628
miriam-gene:2006
,
lld:C0019825
;
a
sio:SIO_001121
.
}
dgn-np:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_provenance
{
dgn-np:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_assertion
dcterms:description
"[We suggest that vocal cord abnormalities may be a far more common feature of WS than has been previously suspected, and that mild vocal cord dysfunction caused by abnormal vocal cord elastin may be the cause of the hoarse voice in this condition.]. 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:12784297
;
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:NP918063.RAQkPV5HzyeSphcgDNrNGKhWYFd3p92xxzEy42nEKjWPY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}