Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_provenance.
- NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_assertion description "[Analysis of 45 episodes of arterial occlusive disease in Japanese patients with congenital protein C deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_provenance.
- NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_assertion evidence source_evidence_literature NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_provenance.
- NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_assertion SIO_000772 10230891 NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_provenance.
- NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_assertion wasDerivedFrom befree-2016 NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_provenance.
- NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_assertion wasGeneratedBy ECO_0000203 NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_provenance.
- befree-2016 importedOn "2016-02-19" NP251822.RAXTU2jUa3i3b74xdMwyHzShz5CnNSUU4gHKbp8MQlYC4130_provenance.