Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_provenance.
- NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_assertion description "[Two recently published studies demonstrated a strong association of genetic variants in the gene that encodes the molecular motor protein nonmuscle myosin 2a (MYH9) with ESRD in African American patients without diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_provenance.
- NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_assertion evidence source_evidence_literature NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_provenance.
- NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_assertion SIO_000772 18923054 NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_provenance.
- NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_assertion wasDerivedFrom befree-20140225 NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_provenance.
- NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_assertion wasGeneratedBy ECO_0000203 NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP727938.RAq8XJ7nM6VPZGeT6qtzu2TQcLG4dkGUwrv1jnuK5M_V4130_provenance.