Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_provenance.
- NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_assertion description "[Several of the top candidate genes include EEF1A1, ROBO1, PLXNA4, SLIT3, NRP1, and NOTCH2, as well as genes associated with the Usher syndrome, PCDH15 and USH2A, and are plausible candidates contributing to the developmental defects in Gbx2(-/-) mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_provenance.
- NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_assertion evidence source_evidence_literature NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_provenance.
- NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_assertion SIO_000772 23144817 NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_provenance.
- NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_assertion wasDerivedFrom befree-20140225 NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_provenance.
- NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_assertion wasGeneratedBy ECO_0000203 NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP564389.RAfj5QPnXpSSx864Wh7JeMEvskGEmOpxA3mMuiE-yL7B4130_provenance.