Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_provenance.
- NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_assertion description "[Mutations at the alpha-globin locus are the most common class of mutations in humans, with deletion of all four adult alpha-globin genes resulting in the perinatal lethal condition haemoglobin Barts hydrops fetalis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_provenance.
- NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_assertion evidence source_evidence_literature NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_provenance.
- NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_assertion SIO_000772 7550311 NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_provenance.
- NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_assertion wasDerivedFrom befree-2016 NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_provenance.
- NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_assertion wasGeneratedBy ECO_0000203 NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1312166.RAq0vcCUlMWN1UEnfDQdVnQt9i8Ujq3lDg16duTkiGEsI130_provenance.