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- NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_assertion type Assertion NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_head.
- NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_assertion wasGeneratedBy ECO_0000203 NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_provenance.
- NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_assertion wasDerivedFrom befree-2016 NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_provenance.
- NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_assertion SIO_000772 22344793 NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_provenance.
- NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_assertion evidence source_evidence_literature NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_provenance.
- NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_assertion description "[Association of X-linked hydrocephalus and Hirschsprung disease: report of a new patient with a mutation in the L1CAM gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961753.RAM3fmeHF4zKdXnfou57DdnpSBmT3VvwvDXnZkPL3-rRE130_provenance.