Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_provenance.
- NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_assertion description "[In contrast, a second group with more severe HbH disease has a non-deletional alpha-thalassemia defect instead of alpha+-thalassemia (genotype alpha alpha T/--SEA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_provenance.
- NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_assertion evidence source_evidence_literature NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_provenance.
- NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_assertion SIO_000772 2762043 NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_provenance.
- NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_assertion wasDerivedFrom befree-2016 NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_provenance.
- NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_assertion wasGeneratedBy ECO_0000203 NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1296627.RAv8r4r9HramSdhL_EVV8gJ7KII6Mpzy9CZ7Ep7DxICfU130_provenance.