Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_provenance.
- NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_assertion description "[A novel mutation of the erythropoietin receptor gene associated with primary familial and congenital polycythaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_provenance.
- NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_assertion evidence source_evidence_literature NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_provenance.
- NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_assertion SIO_000772 21437635 NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_provenance.
- NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_assertion wasDerivedFrom befree-2016 NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_provenance.
- NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_assertion wasGeneratedBy ECO_0000203 NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_provenance.
- befree-2016 importedOn "2016-02-19" NP882313.RANhaEhhJiKXo3wR0Fonv9R5BV7a8aEUXmBbvBq2HaptE130_provenance.