@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms
> .
@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:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_head
{
this:
np:hasAssertion
dgn-np:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_assertion
;
np:hasProvenance
dgn-np:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_provenance
;
np:hasPublicationInfo
dgn-np:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_assertion
a
np:Assertion
.
dgn-np:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_provenance
a
np:Provenance
.
dgn-np:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_assertion
{
miriam-gene:2243
a
ncit:C16612
.
lld:C0001733
a
ncit:C7057
.
dgn-gda:DGN0686661f15c19d847d04a4b4f3e5d64e
sio:SIO_000628
miriam-gene:2243
,
lld:C0001733
;
a
sio:SIO_001121
.
}
dgn-np:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_provenance
{
dgn-np:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_assertion
dcterms:description
"[We report here the identification of 10 novel mutations, of which eight are localized in FGA, thus increasing the total number of causative mutations identified to 72 and confirming the relative importance of FGA in the molecular basis of fibrinogen 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:17295221
;
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:NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}