Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_provenance.
- NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_assertion description "[Our results offer more evidence that in patients with FH, NPHS2-R229Q predisposes to proteinuria and ESKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_provenance.
- NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_assertion evidence source_evidence_literature NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_provenance.
- NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_assertion SIO_000772 22228437 NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_provenance.
- NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_assertion wasDerivedFrom befree-20150227 NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_provenance.
- NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_assertion wasGeneratedBy ECO_0000203 NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP783828.RAe5JRCDbnyoP2flRyGBMI-O1jVBuw1a7-gz8bl8VHS6s130_provenance.