Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance.
- NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance.
- NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_assertion evidence source_evidence_literature NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance.
- NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_assertion SIO_000772 19643772 NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance.
- NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_assertion wasDerivedFrom befree-20140225 NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance.
- NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_assertion wasGeneratedBy ECO_0000203 NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP265654.RAMZs5vKGA5IvuZNVKPmQcJjMG9UMXsDi9HkmaCbxapz8130_provenance.