@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ
> .
@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:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_head
{
this:
np:hasAssertion
dgn-np:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_assertion
;
np:hasProvenance
dgn-np:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_assertion
a
np:Assertion
.
dgn-np:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_provenance
a
np:Provenance
.
dgn-np:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_assertion
{
miriam-gene:3209
a
ncit:C16612
.
lld:C1841679
a
ncit:C7057
.
dgn-gda:DGN35ecdb2c26a389ac5f22630990913c37
sio:SIO_000628
miriam-gene:3209
,
lld:C1841679
;
a
sio:SIO_001121
.
}
dgn-np:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_provenance
{
dgn-np:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_assertion
dcterms:description
"[When patients present with septa, it is not necessary to subject them to roentgenograms of the distal limbs or to sequence analysis of HOXA13 unless they show clear signs of the other sequelae characteristic of true HFGS.]. 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:19591980
;
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:NP626562.RAIHTIITuntbBD7Bi89cq2LnqMVn2Bi0h8lmmXSPMMvdQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:18+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" .
}