Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance.
- NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance.
- NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_assertion evidence source_evidence_literature NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance.
- NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_assertion SIO_000772 23559863 NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance.
- NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_assertion wasDerivedFrom befree-20150227 NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance.
- NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_assertion wasGeneratedBy ECO_0000203 NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance.