@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc
> .
@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:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_head
{
this:
np:hasAssertion
dgn-np:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_assertion
;
np:hasProvenance
dgn-np:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_provenance
;
np:hasPublicationInfo
dgn-np:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_assertion
a
np:Assertion
.
dgn-np:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_provenance
a
np:Provenance
.
dgn-np:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_assertion
{
miriam-gene:1351
a
ncit:C16612
.
lld:C0242666
a
ncit:C7057
.
dgn-gda:DGN5ae126784ac10910a1b47b4019d7710a
sio:SIO_000628
miriam-gene:1351
,
lld:C0242666
;
a
sio:SIO_001121
.
}
dgn-np:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_provenance
{
dgn-np:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_assertion
dcterms:description
"[Beside the frequent polymorphism already described on Pro 626, we detected 18 different sequence variations by studying exons II, IV, V, VIII, X, and XV in 19 of 100 consecutive patients with protein S 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:7803790
;
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:NP464829.RAXPtHMVMEG3TD4naAzc4Q_kzjq3gC6rZW43fzGsX6sbc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:39+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" .
}