Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_provenance.
- NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_assertion description "[Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) can both be due to mutations in the genes encoding ?-myosin heavy chain (MYH7) or cardiac myosin-binding protein C (MYBPC3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_provenance.
- NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_assertion evidence source_evidence_literature NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_provenance.
- NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_assertion SIO_000772 21750094 NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_provenance.
- NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_assertion wasDerivedFrom befree-20150227 NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_provenance.
- NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_assertion wasGeneratedBy ECO_0000203 NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP696443.RAAwleUhS9G2TLJHg-aDtopI7S4IGNmUIFZnEOcSulp3Q130_provenance.