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- source_evidence_literature type ECO_0000212 NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_provenance.
- NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_provenance.
- NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_assertion evidence source_evidence_literature NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_provenance.
- NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_assertion SIO_000772 19247433 NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_provenance.
- NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_assertion wasDerivedFrom befree-20150227 NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_provenance.
- NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_assertion wasGeneratedBy ECO_0000203 NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_provenance.