@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg
> .
@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:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_head
{
this:
np:hasAssertion
dgn-np:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_assertion
;
np:hasProvenance
dgn-np:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_provenance
;
np:hasPublicationInfo
dgn-np:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_assertion
a
np:Assertion
.
dgn-np:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_provenance
a
np:Provenance
.
dgn-np:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0007789
a
ncit:C7057
.
dgn-gda:DGNe635c00abbee2c4a0bce51b97a537882
sio:SIO_000628
miriam-gene:2153
,
lld:C0007789
;
a
sio:SIO_001121
.
}
dgn-np:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_provenance
{
dgn-np:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_assertion
dcterms:description
"[The frequency of the fVL mutation in children with evidence of vascular thrombosis and their mothers was not statistically different from the frequency in children with CP with other imaging findings and their mothers.]. 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:16359589
;
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:NP154721.RAUeyp8v3jNFaV_hn4aiJl7jR9vrXVaJqHfqLhYwLgusg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:22+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" .
}