@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM
> .
@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:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_head
{
this:
np:hasAssertion
dgn-np:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_assertion
;
np:hasProvenance
dgn-np:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_provenance
;
np:hasPublicationInfo
dgn-np:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_assertion
a
np:Assertion
.
dgn-np:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_provenance
a
np:Provenance
.
dgn-np:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_assertion
{
miriam-gene:7056
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGNc186bb1467b3a54bb8a889df04a8b51c
sio:SIO_000628
miriam-gene:7056
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_provenance
{
dgn-np:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_assertion
dcterms:description
"[This work presents biochemical evidence that certain (but not all) natural mutations in the TM gene reduce expression and impair function of the protein on the cell surface, and helps clarify the suggested contribution that these mutations might make to the risk of thromboembolic disease.]. 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:11986219
;
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:NP719380.RAYjttohjsMvQMTNmN2kpE5BhM_iJt9eMk8KimrwzKQoM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}