@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ
> .
@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:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_head
{
this:
np:hasAssertion
dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_assertion
;
np:hasProvenance
dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_assertion
a
np:Assertion
.
dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_provenance
a
np:Provenance
.
dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_assertion
{
miriam-gene:1351
a
ncit:C16612
.
lld:C0023895
a
ncit:C7057
.
dgn-gda:DGN8d9810aa9a12f4f5ef5158630d423623
sio:SIO_000628
miriam-gene:1351
,
lld:C0023895
;
a
sio:SIO_001121
.
}
dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_provenance
{
dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_assertion
dcterms:description
"[Patients with CRF had a similar distribution to those with chronic liver diseases, whilst the greatest diversity of genotypes was seen in patients with haemophilia, which was expected since they were given factor VIII manufactured overseas.]. 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:9744672
;
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:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:39+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" .
}