@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI
> .
@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:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_head
{
this:
np:hasAssertion
dgn-np:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_assertion
;
np:hasProvenance
dgn-np:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_provenance
;
np:hasPublicationInfo
dgn-np:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_assertion
a
np:Assertion
.
dgn-np:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_provenance
a
np:Provenance
.
dgn-np:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_assertion
{
miriam-gene:5340
a
ncit:C16612
.
lld:C1260903
a
ncit:C7057
.
dgn-gda:DGN5be0c861c2c40f57bcb1558b04070041
sio:SIO_000628
miriam-gene:5340
,
lld:C1260903
;
a
sio:SIO_001121
.
}
dgn-np:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_provenance
{
dgn-np:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_assertion
dcterms:description
"[Three families with antithrombin deficiency, 35 with protein C, 60 with protein S, four with plasminogen, four with heparin cofactor II, seven with combined deficiencies and one family with dysfibrinogenemia were included in the analysis.]. 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:9607121
;
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:NP682032.RAX-m3jVNjhoQ3Ro14VfyM559_88F2pRQ-UJJ4giipQOI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:51+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" .
}