Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_provenance.
- NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_assertion description "[We identified 75 different LDL receptor mutations in 645 children with heterozygous FH; in these children, null alleles were clearly associated with more elevated LDL cholesterol levels compared to receptor-defective mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_provenance.
- NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_assertion evidence source_evidence_literature NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_provenance.
- NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_assertion SIO_000772 15823280 NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_provenance.
- NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_assertion wasDerivedFrom befree-2016 NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_provenance.
- NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_assertion wasGeneratedBy ECO_0000203 NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP489375.RAS6SRo5HA7TLyxVUYzscxc3VvHA_qNzgh6vLjLxGKbjQ130_provenance.