@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs
> .
@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:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_head
{
this:
np:hasAssertion
dgn-np:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_assertion
;
np:hasProvenance
dgn-np:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_provenance
;
np:hasPublicationInfo
dgn-np:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_assertion
a
np:Assertion
.
dgn-np:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_provenance
a
np:Provenance
.
dgn-np:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_assertion
{
miriam-gene:9464
a
ncit:C16612
.
lld:C0162359
a
ncit:C7057
.
dgn-gda:DGNfb70f9be2eb9a39148f5d5cba5b98d92
sio:SIO_000628
miriam-gene:9464
,
lld:C0162359
;
a
sio:SIO_001121
.
}
dgn-np:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_provenance
{
dgn-np:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_assertion
dcterms:description
"[The aim of this work is to present the analysis of dental traits in five families (affected boys and their mothers) with hypohidrotic ectodermal dysplasia (HED), and to evaluate the importance of orofacial and dental findings in the determination of female HED gene carriers.]. 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:11787554
;
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:NP193972.RATXuVTToIK4mG1PX2XGBH9P4HsFG6Rp2dcLp_x3vI7vs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}