Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP961912.RAYtZadeYcXpA19nJUF_gkRuuvCwQBbpEG_iVh-A7atbY130_provenance.
- 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.