http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#head
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#assertion
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#provenance
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#assertion
http://rdf.disgenet.org/resource/gda/DGNd6168877781e13e321387cb8307f5c65
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/7291
http://rdf.disgenet.org/resource/gda/DGNd6168877781e13e321387cb8307f5c65
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0010278
http://rdf.disgenet.org/resource/gda/DGNd6168877781e13e321387cb8307f5c65
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#provenance
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#assertion
http://purl.org/dc/terms/description
[Between 30% and 70% of syndromic craniosynostoses are caused by mutations in hotspots in the fibroblast growth factor receptor (FGFR) genes or in the TWIST1 gene with the difference in detection rates likely to be related to different study populations within craniofacial centers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#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/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/24127277
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#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/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/dc/terms/created
2017-10-17T13:17:07+02:00
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1085619.RAwi7QlTkXB20znPCakYMVNiuJ3wHIxprVBcXL60LX5mY
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