Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_assertion> ?p ?o ?g. }
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- NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_assertion type Assertion NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_head.
- NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_assertion wasGeneratedBy ECO_0000203 NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_provenance.
- NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_assertion wasDerivedFrom befree-20140225 NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_provenance.
- NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_assertion SIO_000772 17943323 NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_provenance.
- NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_assertion evidence source_evidence_literature NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_provenance.
- NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_assertion description "[This observation, together with two recent reports on milder variants of Pierson syndrome, corroborates the concept that the clinical expression of Pierson syndrome is more variable than initially described, and that milder phenotypes may be related to hypomorphic LAMB2 alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475245.RAWvGSPe7mvNviaIpNX9qM0Vt__7EHlLRpOhz1f1Y42H4130_provenance.