Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_provenance.
- befree-2016 importedOn "2016-02-19" NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_provenance.
- NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_assertion wasGeneratedBy ECO_0000203 NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_provenance.
- NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_assertion wasDerivedFrom befree-2016 NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_provenance.
- NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_assertion SIO_000772 10925378 NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_provenance.
- NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_assertion evidence source_evidence_literature NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_provenance.
- NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_assertion description "[The DFNA2 locus for autosomal dominant nonsyndromic hearing impairment on chromosome 1p34 contains at least 2 genes responsible for hearing loss, GJB3 and KCNQ4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP290795.RAm0lFM7DCLLBLAGlz0uYjxY3CDxLgOBfpQf9XClVeUD8130_provenance.