http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#head
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#assertion
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#provenance
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#assertion
http://rdf.disgenet.org/resource/gda/DGNd996f9c02cc87b1dc8c252009e743616
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/7248
http://rdf.disgenet.org/resource/gda/DGNd996f9c02cc87b1dc8c252009e743616
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0029434
http://rdf.disgenet.org/resource/gda/DGNd996f9c02cc87b1dc8c252009e743616
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#provenance
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#assertion
http://purl.org/dc/terms/description
[Eleven paternal diseases were discovered, which were Noonan-like syndrome (1), paternal cervical anomalies (1), Goldenhar syndrome (1), dominant autosomal arthrogryposis (1), osteogenesis imperfecta (3), tuberous sclerosis (1), dominant transposition of great vessels (1), Weyers acrofacial dysostosis (1), and autosomal dominant holoprosencephaly (1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#assertion
http://purl.org/ontology/wi/core#evidence
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/17139695
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://purl.org/pav/importedOn
2017-02-19
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.obolibrary.org/obo/ECO_0000212
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#comment
Gene-disease associations inferred from text-mining the literature.
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#label
DisGeNET evidence - LITERATURE
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/dc/terms/created
2017-10-17T13:17:03+02:00
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1077454.RAYGVwq61MBI7qIw-e3f25aJzi1NsyABM19Ap-set0kZo
http://purl.org/pav/version
v5.0.0.0
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://purl.org/pav/version
v5.0.0