Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_assertion> ?p ?o ?g. }
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- NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_assertion type Assertion NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_head.
- NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_assertion description "[The ataxia telangiectasia mutated-Rad3 related (ATR)-Chk1 pathway is defective in Seckel syndrome, another microcephaly disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_provenance.
- NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_assertion evidence source_evidence_literature NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_provenance.
- NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_assertion SIO_000772 16217032 NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_provenance.
- NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_assertion wasDerivedFrom befree-20150227 NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_provenance.
- NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_assertion wasGeneratedBy ECO_0000203 NP312878.RAuIsb2XTBWz2DfwFjdtRAD5VhpEKtHLeD1wnevYLB6EU130_provenance.