@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY
> .
@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:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_head
{
this:
np:hasAssertion
dgn-np:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_assertion
;
np:hasProvenance
dgn-np:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_provenance
;
np:hasPublicationInfo
dgn-np:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_assertion
a
np:Assertion
.
dgn-np:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_provenance
a
np:Provenance
.
dgn-np:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_assertion
{
miriam-gene:2152
a
ncit:C16612
.
lld:C0015526
a
ncit:C7057
.
dgn-gda:DGN07085efda86f3fec3a1d7f3955232bcd
sio:SIO_000628
miriam-gene:2152
,
lld:C0015526
;
a
sio:SIO_001121
.
}
dgn-np:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_provenance
{
dgn-np:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_assertion
dcterms:description
"[Additionally, activated partial thromboplastin time (APTT) of the patient was disproportionately prolonged and there were reduced levels of coagulation factor XII in the patients and members of the maternal trait which are compatible with heterozygous factor XII deficiency.]. 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:1550105
;
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:NP604244.RAB6sXgkV2h2egvnAe9TkQkmRU61tjr9u9m0iqKwCyovY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:03+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" .
}