Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_provenance.
- NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_assertion description "[Single nucleotide polymorphisms and haplotypes analysis of DFNB1 locus in Chinese sporadic hearing impairment population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_provenance.
- NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_assertion evidence source_evidence_literature NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_provenance.
- NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_assertion SIO_000772 19719946 NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_provenance.
- NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_assertion wasDerivedFrom gad-20150221 NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_provenance.
- NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_assertion wasGeneratedBy ECO_0000203 NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP155633.RAhGx_nSedAD-Fa2vMmeKA2vSIzTCEAtOz1RZ98wNpHjw130_provenance.