Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_provenance.
- NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_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." NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_provenance.
- NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_assertion evidence source_evidence_literature NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_provenance.
- NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_assertion SIO_000772 21712856 NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_provenance.
- NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_assertion wasDerivedFrom befree-20140225 NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_provenance.
- NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_assertion wasGeneratedBy ECO_0000203 NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP190196.RAeg5GbNETadoiM-nkGfQr48oxxX-pOx2TEnSY_g-arAg130_provenance.