Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_provenance.
- NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_assertion description "[The family contained three members homozygous for C6 deficiency (C6D); two of them were deficient also in factor VIII.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_provenance.
- NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_assertion evidence source_evidence_literature NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_provenance.
- NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_assertion SIO_000772 6811172 NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_provenance.
- NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_assertion wasDerivedFrom befree-2016 NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_provenance.
- NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_assertion wasGeneratedBy ECO_0000203 NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1307005.RAtI2F5yx8CWqp9wfn_AeKiMOh5bNNZWZh1LX7FlFOTgQ130_provenance.