Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_provenance.
- NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_assertion description "[Haptoglobin (Hp) polymorphism generates three common human genotypes (Hp1-1, Hp2-1, and Hp2-2), having functional differences, related to the risk of development of cardiovascular diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_provenance.
- NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_assertion evidence source_evidence_literature NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_provenance.
- NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_assertion SIO_000772 24535155 NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_provenance.
- NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_assertion wasDerivedFrom befree-20150227 NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_provenance.
- NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_assertion wasGeneratedBy ECO_0000203 NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP983613.RAb0usNu9Mbe-4B6lQX7gMTBTq_gr7rc3rVdMyhe-IcFE130_provenance.