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- NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_assertion type Assertion NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_head.
- NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_assertion wasGeneratedBy ECO_0000203 NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_provenance.
- NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_assertion wasDerivedFrom befree-20150227 NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_provenance.
- NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_assertion SIO_000772 23171239 NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_provenance.
- NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_assertion evidence source_evidence_literature NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_provenance.
- NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_assertion description "[Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_provenance.