Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance.
- NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_assertion description "[The aims of this study were (i) to investigate the association of single nucleotide polymorphisms within the TNC gene, and the additional candidate gene, COL27A1, with AT in two populations, and (ii) to identify if there is a risk haplotype for AT in both populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance.
- NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_assertion evidence source_evidence_literature NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance.
- NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_assertion SIO_000772 23192621 NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance.
- NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_assertion wasDerivedFrom befree-20140225 NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance.
- NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_assertion wasGeneratedBy ECO_0000203 NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance.