Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_provenance.
- NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_assertion description "[Hereditary deficiency of C1 esterase inhibitor (C1 INH) responsible for hereditary angioedema (HAE) is the most common hereditary complement deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_provenance.
- NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_assertion evidence source_evidence_literature NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_provenance.
- NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_assertion SIO_000772 2736814 NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_provenance.
- NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_assertion wasDerivedFrom befree-20140225 NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_provenance.
- NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_assertion wasGeneratedBy ECO_0000203 NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP821293.RA7b2Vd2C8s9Af8tSHn7oYWsGUR1EihSVb7DkIKs8ipJA130_provenance.