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- source_evidence_literature type ECO_0000212 NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_provenance.
- NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_assertion wasGeneratedBy ECO_0000203 NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_provenance.
- NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_assertion wasDerivedFrom befree-20150227 NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_provenance.
- NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_assertion SIO_000772 11561226 NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_provenance.
- NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_assertion evidence source_evidence_literature NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_provenance.
- NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_assertion description "[Novel rod segment mutations in lamin A/C cause variable conduction system disease and dilated cardiomyopathy without skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537866.RAMinSZ4rdfAalfB49cfnQ9MKLYpn5CC2_izT4ByB6Y3Q130_provenance.