Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_provenance.
- NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_assertion description "[The PITX3 gene, which codes for a homeobox bicoidlike transcription factor is responsible for dominant cataract and anterior segment mesenchymal dysgenesis in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_provenance.
- NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_assertion evidence source_evidence_literature NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_provenance.
- NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_assertion SIO_000772 16565358 NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_provenance.
- NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_assertion wasDerivedFrom befree-20140225 NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_provenance.
- NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_assertion wasGeneratedBy ECO_0000203 NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP816218.RA58bAVsglMIOPxah1KpgOTUgXXSEhw6rUxac3utNUddU130_provenance.