Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_provenance.
- NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_assertion description "[The LCCL module of coch-5b2 is of special biological interest because it has been shown recently that mutations affecting this module cause the deafness disorder DFNA9 in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_provenance.
- NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_assertion evidence source_evidence_literature NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_provenance.
- NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_assertion SIO_000772 10971586 NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_provenance.
- NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_assertion wasDerivedFrom befree-20140225 NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_provenance.
- NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_assertion wasGeneratedBy ECO_0000203 NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP250912.RASl0XFkMdexU0pXwkDst9LrBIj0spL9yeDQJdAI_j3tU130_provenance.