@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc
> .
@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:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_head
{
this:
np:hasAssertion
dgn-np:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_assertion
;
np:hasProvenance
dgn-np:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_provenance
;
np:hasPublicationInfo
dgn-np:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_assertion
a
np:Assertion
.
dgn-np:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_provenance
a
np:Provenance
.
dgn-np:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_assertion
{
miriam-gene:2155
a
ncit:C16612
.
lld:C0020255
a
ncit:C7057
.
dgn-gda:DGN65d5d82ef3b01a5946f6d3a0331250ad
sio:SIO_000628
miriam-gene:2155
,
lld:C0020255
;
a
sio:SIO_001121
.
}
dgn-np:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_provenance
{
dgn-np:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_assertion
dcterms:description
"[We report a family with high consanguineous relations, who experienced death of two baby girls, the first with prenatal manifestation of foetal hydrocephalus secondary to intracranial bleeding and the second with postnatal intracranial bleeding, both with less than 1% activity of FVII.]. 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:19432927
;
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:NP527396.RAFOl5eSKx5pCcWG2zfvQwTRWr260kZ8oT-xwC7YgHzUc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:16+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" .
}