Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_provenance.
- NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_assertion description "[This is the second known instance of a male infant with omphalocele and this skeletal dysplasia born to a woman with MNS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_provenance.
- NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_assertion evidence source_evidence_literature NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_provenance.
- NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_assertion SIO_000772 7158644 NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_provenance.
- NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_assertion wasDerivedFrom befree-20150227 NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_provenance.
- NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_assertion wasGeneratedBy ECO_0000203 NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP406945.RA4iG5I5Fn9B0dMsVhidsrD0UJWZV8Qj2Sz8ibtqeR-Wc130_provenance.