Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_provenance.
- NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_assertion description "[MLP is therefore a candidate gene for heritable forms of hypertrophic cardiomyopathy (HCM) and DCM in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_provenance.
- NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_assertion evidence source_evidence_literature NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_provenance.
- NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_assertion SIO_000772 12642359 NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_provenance.
- NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_assertion wasDerivedFrom befree-20150227 NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_provenance.
- NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_assertion wasGeneratedBy ECO_0000203 NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788970.RAd436FLSdFbJF-2ui2-OI6AaNbJVSheDi1gNxWTpG8kE130_provenance.