Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_provenance.
- NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_assertion description "[The nosological classification of this disease has been debated as the condition shares features common to other skeletal dysplasias such as Melnick Needles syndrome (MNS; MIM309350) and Hajdu-Cheney Syndrome (HCS; MIM102500).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_provenance.
- NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_assertion evidence source_evidence_literature NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_provenance.
- NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_assertion SIO_000772 21712856 NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_provenance.
- NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_assertion wasDerivedFrom befree-20140225 NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_provenance.
- NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_assertion wasGeneratedBy ECO_0000203 NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP908621.RAtkG5wtyBdDIkJLROUv_qN116wP9E8OxusEmeXIZr-dY130_provenance.