@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_head
{
this:
np:hasAssertion
dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_assertion
;
np:hasProvenance
dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_provenance
;
np:hasPublicationInfo
dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_assertion
a
np:Assertion
.
dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_provenance
a
np:Provenance
.
dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0034065
a
ncit:C7057
.
dgn-gda:DGN3ae0e5f8d2a33aac16e74aa84bee7e15
sio:SIO_000628
miriam-gene:4524
,
lld:C0034065
;
a
sio:SIO_001122
.
}
dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_provenance
{
dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_assertion
dcterms:description
"[, coagulant factor V gene G1691A mutation and prothrombin G20210A mutation are very rare, while MTHFR C677T mutation is very common, and all of them are not associated with pulmonary thromboembolism in the Chinese population.]. 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:12165282
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:30+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}