Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_provenance.
- NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_assertion description "[CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_provenance.
- NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_assertion evidence source_evidence_literature NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_provenance.
- NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_assertion SIO_000772 19021638 NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_provenance.
- NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_assertion wasDerivedFrom befree-2016 NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_provenance.
- NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_assertion wasGeneratedBy ECO_0000203 NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_provenance.
- befree-2016 importedOn "2016-02-19" NP704844.RABY0PLn8rKhnt8KMbXjUQBXA32w0JTOYNATQNAZiBNCc130_provenance.