@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE
> .
@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:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_head
{
this:
np:hasAssertion
dgn-np:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_assertion
;
np:hasProvenance
dgn-np:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_provenance
;
np:hasPublicationInfo
dgn-np:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_assertion
a
np:Assertion
.
dgn-np:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_provenance
a
np:Provenance
.
dgn-np:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0034152
a
ncit:C7057
.
dgn-gda:DGN0b6b8297694ba75fd082fc948b68e9f8
sio:SIO_000628
miriam-gene:2147
,
lld:C0034152
;
a
sio:SIO_001121
.
}
dgn-np:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_provenance
{
dgn-np:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_assertion
dcterms:description
"[Based on the hypothesis that an inherited predilection to hypercoagulability may predispose to HSP or may mark those who develop acute clinical manifestations, we evaluated the possible roles of methylenetetrahydrofolate reductase (MTHFR) gene C677T, factor V (FV) gene G1691A (Leiden), and prothrombin gene G20210A polymorphisms in patients with HSP.]. 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:16791607
;
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:NP918810.RASowLMF5GOfZgZZfFXC0Ke-gH0NYLIJ_rl1GBz22s5YE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:24+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" .
}