@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_head
{
this:
np:hasAssertion
dgn-np:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_assertion
;
np:hasProvenance
dgn-np:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_provenance
;
np:hasPublicationInfo
dgn-np:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_assertion
a
np:Assertion
.
dgn-np:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_provenance
a
np:Provenance
.
dgn-np:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_assertion
{
miriam-gene:157570
a
ncit:C16612
.
lld:C0376634
a
ncit:C7057
.
dgn-gda:DGN7ab3a4a7c3e596df65d5cfd6e2b5d42f
sio:SIO_000628
miriam-gene:157570
,
lld:C0376634
;
a
sio:SIO_001121
.
}
dgn-np:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_provenance
{
dgn-np:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_assertion
dcterms:description
"[To determine whether ESCO2 mutations are also responsible for SC, we studied three families with SC and two families in which variable degrees of limb and craniofacial abnormalities, detected by fetal ultrasound, led to pregnancy terminations.]. 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:16380922
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP976667.RANyY3m6mBDPjWhFSkwTnD8qpxAj8ZTxbSgoX5qKiK4Zw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:36+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}