@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4
> .
@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:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_head
{
this:
np:hasAssertion
dgn-np:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_assertion
;
np:hasProvenance
dgn-np:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_provenance
;
np:hasPublicationInfo
dgn-np:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_assertion
a
np:Assertion
.
dgn-np:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_provenance
a
np:Provenance
.
dgn-np:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_assertion
{
miriam-gene:3858
a
ncit:C16612
.
lld:C0239849
a
ncit:C7057
.
dgn-gda:DGNd93540bc0cc2b8a46dce5fbddbbf8e41
sio:SIO_000628
miriam-gene:3858
,
lld:C0239849
;
a
sio:SIO_001121
.
}
dgn-np:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_provenance
{
dgn-np:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_assertion
dcterms:description
"[These technics have been utilized successfully in the prenatal diagnosis or exclusion of epidermolysis bullosa, epidermolytic hyperkeratosis, and harlequin ichthyosis in fetuses known to be at risk for these disorders, and they offer tremendous potential for prenatal diagnosis in a variety of other genodermatoses.]. 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:6863622
;
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:NP874027.RA7tWNSvED9mkSsluHbQT9jh6Zq5u9x2KLyARXZboBtn4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}