@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE
> .
@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:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_head
{
this:
np:hasAssertion
dgn-np:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_assertion
;
np:hasProvenance
dgn-np:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_provenance
;
np:hasPublicationInfo
dgn-np:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_assertion
a
np:Assertion
.
dgn-np:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_provenance
a
np:Provenance
.
dgn-np:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_assertion
{
miriam-gene:780896
a
ncit:C16612
.
lld:C0019555
a
ncit:C7057
.
dgn-gda:DGNb6c94717c797c15c8a7097578c4893de
sio:SIO_000628
miriam-gene:780896
,
lld:C0019555
;
a
sio:SIO_001121
.
}
dgn-np:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_provenance
{
dgn-np:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_assertion
dcterms:description
"[The fact that acetabular development in the family members who did not have congenital dysplasia of the hip was no different from that in the control subjects suggests that acetabular dysplasia, rather than being an inherited abnormality, is secondary to subluxation or dislocation.]. 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:2254359
;
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:NP688108.RAMqCsZ8OqrPSH_mZa6JMPK_QnUBeLztZ0tIMkLvWPfsE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}