Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_provenance.
- befree-20150227 importedOn "2015-02-27" NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_provenance.
- NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_assertion wasGeneratedBy ECO_0000203 NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_provenance.
- NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_assertion wasDerivedFrom befree-20150227 NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_provenance.
- NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_assertion SIO_000772 22050868 NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_provenance.
- NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_assertion evidence source_evidence_literature NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_provenance.
- NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_assertion description "[Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961910.RAA6jOsTSsKyRW_aUURO_KS3jIsEBv9Wep_Dazs3K3V94130_provenance.