Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_provenance.
- NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_assertion wasGeneratedBy ECO_0000203 NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_provenance.
- NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_assertion wasDerivedFrom befree-20150227 NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_provenance.
- NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_assertion SIO_000772 8931691 NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_provenance.
- NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_assertion evidence source_evidence_literature NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_provenance.
- NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_assertion description "[This study reports 12 novel mutations of the Wilson disease (WD) gene which have been detected by the molecular analysis of 29 patients of Mediterranean descent carrying uncommon chromosomal haplotypes at the WD locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697260.RAPw02Y9BepMBRINg35DNPcUXfkdA3i2fm2gEQdEslkbk130_provenance.