Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_provenance.
- NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_assertion description "[The SLC26A11 gene mapped to human chromosome 17q25, very close to the hereditary hearing loss diseases loci DFNA20, DFNA26, and USH1G.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_provenance.
- NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_assertion evidence source_evidence_literature NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_provenance.
- NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_assertion SIO_000772 12626430 NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_provenance.
- NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_assertion wasDerivedFrom befree-20140225 NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_provenance.
- NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_assertion wasGeneratedBy ECO_0000203 NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP751878.RATkivqMaGxK-3KR1GTxM7QMYPe4mo99EQy68ZFbfMblw130_provenance.